BACULOVIRUS-BASED PRODUCTION OF BIOPHARMACEUTICALS FREE OF CONTAMINATING BACULOVIRAL VIRIONS

Abstract

The present invention relates to methods for the production of biopharmaceuticals implementing a baculovirus-based system. These methods advantageously allow the production of biopharmaceuticals with a reduced number of or without contaminating baculoviral virions.

Description

CROSS-REFERENCE TO RELATED APPLICATIONS

[0001] This application is a continuation of U.S. Ser. No. 15/841,359, filed Dec. 14, 2017, which is a continuation of U.S. Ser. No. 14/670,459, filed Mar. 27, 2015, now U.S. Pat. No. 9,862,934, which is a continuation of U.S. Ser. No. 13/390,806, filed Feb. 16, 2012, now U.S. Pat. No. 8,993,317, which is the U.S. national stage application of International Patent Application No. PCT/EP2010/061456, filed Aug. 5, 2010, the disclosures of which are hereby incorporated by reference in their entirety, including all figures, tables and amino acid or nucleic acid sequences.

[0002] The Sequence Listing for this application is labeled "Seq-List.txt" which was created on Feb. 9, 2012 and is 117 KB. The entire contents of the sequence listing is incorporated herein by reference in its entirety.

[0003] The present invention relates to methods for the production of biopharmaceuticals implementing a baculovirus-based system. These methods advantageously allow the production of biopharmaceuticals with reduced or no contaminating baculoviral virions.

[0004] Over the past two decades the baculovirus-insect cell technology has become a very frequently used eukaryotic expression system for the production of recombinant proteins, not only for scientific purposes, but more and more for human and veterinary medicine (Condreay and Kost, 2007, van Oers, 2006). In particular, recombinant baculoviruses derived from Autographa californica multicapsid nucleopolyhedrovirus (AcMNPV) are widely employed for large-scale production of heterologous proteins in cultured insect cells. The main reasons for the frequent application of this system are: (1) high levels of expression of foreign proteins, (2) insect cells are able to grow in a suspension culture and thus are easy to scale up, (3) the proteins synthesized in insect cells are processed and modified post-translationally, (4) well-developed manipulation techniques for the viral vectors resulting in a flexible expression system, and 5) non-pathogenic to humans, as the baculovirus host range is restricted to insects and invertebrates. Recombinant baculovirus vectors are being used for the production of individual proteins, as for sub-unit vaccine purposes, but also for higher order structures containing one or more proteins, such as enzyme complexes, viruses or virus-like particles.

[0005] Virus-like particles (VLPs) are highly organised structures that self-assemble from virus-derived structural proteins. These stable and versatile nano-particles possess excellent adjuvant properties capable of inducing innate and acquired immune responses (Ludwig & Wagner, 2007). During the past years, VLPs have been applied in other branches of biotechnology taking advantage of their structural stability and tolerance towards manipulation to carry and display heterologous molecules or serve as building blocks for novel nanomaterials. For immuno-therapeutic and prophylactic applications, many types of virus-like particles (VLP) have been successfully produced in baculovirus-infected insect cells (Noad & Roy, 2003, van Oers et al., 2006, Ramqvist et al., 2007). The first commercial achievement of baculovirus VLP technology for use in humans is the human papillomavirus (HPV) vaccine recently marketed by GlaxoSmithKline, prophylactic against HPV strains 16 and 18. The L1 protein of each of these types of HPV was expressed via a recombinant baculovirus vector and the resulting VLPs were combined to produce the vaccine Cervarix.TM. (Harper et al., 2006).

[0006] Today, there is a huge effort to develop baculovirus-derived influenza virus-like particles as well as influenza subunit-vaccines as a new generation of non-egg and non-mammalian cell culture-based candidate vaccine. Non-replicating influenza virus-like particles are effective in eliciting a broadened, cross-clade protective immune response to proteins from emerging H5N1 influenza isolates giving rise to a potential pandemic influenza vaccine candidate for humans that can be stockpiled for use in the event of an outbreak of H5N1 influenza (Bright et al., 2008). An influenza subunit vaccine produced in insect cells is close to FDA approval (Cox and Hollister, 2009). Similar strategies could in principle be applied for vaccines against the pandemic influenza such as the recent outbreak of Swine flu.

[0007] For gene therapy purposes, baculovirus-insect cell technology is also being applied for the production of infectious adeno-associated virus vectors (e.g. Urabe et al., 2002) and lentiviral vectors (Lesch et al., 2008). For the production of AAV vectors insect cells are co-infected with three recombinant baculoviruses--one producing the AAV replicase (REP) proteins, one carrying the cap functions for producing the AAV viral structural proteins (VP1, VP2. VP3), and a third baculovirus comprising an AAV-ITR vector with the ability to carry and transfer transgenes. Recently an improved version of this production had been published which is based on the use of only recombinant baculoviruses, one of them carrying the rep and cap functions of AAV (Smith et al. 2009). The produced AAV vector is indistinguishable from that produced in mammalian cells in its physical and biological properties. The yield of the AAV-ITR vector particles approached 5.times.10.sup.4 per Sf9 insect cell demonstrating that the system is able to produce high quantities of AAV vectors in a simple manner. Currently, clinical trials with baculovirus-derived AAV vectors are underway for instance for lipoprotein lipase deficiency (Amsterdam Molecular Therapeutics B.V.). As an alternative, scalable approach to produce lentiviral vectors (Lesch et al., 2008) mammalian 293T cells were transduced simultaneously by four recombinant baculoviruses produced in insect cells to express all elements required for generation of a safe lentivirus vector. The unconcentrated lentiviral titers in mammalian cell culture media were on average 2.5.times.10.sup.6 TU ml.sup.-1, comparable to titers of the lentiviruses produced by conventional four-plasmid transfection methods. In addition, there is a general effort to convert lentiviral vector production methods into better scalable insect cell-based technologies.

[0008] Tjia et al., 1983 discovered that BVs can be internalized by mammalian cells and even some of the viral DNA reached the cell nucleus. Further studies showed that baculoviruses can enter mammalian cells and mediate expression of Escherichia coli chloramphenicol acetyl-transferase under the Rous sarcoma virus promoter (Carbonell et al., 1985). These findings led to the development of novel baculovirus-based gene delivery vehicles for mammalian cells (Boyce & Bucher, 1996, Hofmann et al., 1995, Condreay and Kost, 2007, Kaikkonen et al., 2008). Today, there is strong evidence that baculovirus-derived gene delivery vectors can mediate transient and stable expression of foreign genes in mammalian cells following antibiotic selection (Lackner et al., 2008).

[0009] There is still poor knowledge about transcriptional activities of baculovirus promoters in mammalian cells. It has been demonstrated that the transactivator protein IE1 of AcMNPV is functional in mammalian cells (Murges et al., 1997) as well as the early-to-late (ETL) promoter (Liu et al., 2006a,b). Among the other imperfectly explored areas is the interaction of baculoviruses with components of the mammalian immune system. AcMNPV virus is able to induce antiviral cytokine production, which protects cells from infection with vesicular stomatitis virus and influenza virus (Abe et al., 2003, Gronowski et al., 1999). AcMNPV is also recognized by Toll-like receptor 9 on dendritic cells and macrophages, and AcMNPV induces antitumor acquired immunity (Kitajima & Takaku, 2008). These results suggest that AcMNPV has the potential to be an efficient virus or tumor therapy agent which induces innate and acquired immunity. In spite of universally positive effects of AcMNPV on components of the humoral and adaptive cell-mediated immunity in mice, the interaction of baculoviruses with the human immune system can be slightly different. Additionally, immunoadjuvant properties of AcMNPV should be fully separated from immune response against target vaccine/biopharmaceuticals produced in insect cells.

[0010] These features of baculoviruses are strongly disadvantageous in cases where baculoviruses are utilized for the production of vaccines or viral vectors for therapeutical purposes (e.g. AAV, lentivirus). Contamination of the produced biopharmaceuticals with both types of baculovirus virions--budded virions (BVs) and occlusion-derived virions (ODVs) should, therefore, be avoided. In general, the recombinant proteins can be produced in insect cells as cytosolic, membrane-bound, or extra-cellularly secreted proteins. The latter secreted proteins are highly "contaminated" with baculoviral BVs present in the culture medium. It can be very difficult to separate undesirable baculovirus virions from produced recombinant biopharmaceuticals in some production and purification configurations. It has been shown for instance that these BVs can cause problems during the purification process of AAV vectors produced with baculovirus-insect cell technology (personal communication O. Merten, Genethon). On the other hand, there are also ODVs, always formed inside the nuclei of infected cells, in all conventional baculovirus-insect cell expression systems, even if occlusion bodies are not formed, due to replacement of the polyhedrin open reading frame by a desired gene. Analogously, these virions can co-purify with intracellularly produced recombinant proteins or VLPs during purification process.

[0011] In summary, the separation of recombinant proteins and, especially, VLPs from baculovirus particles, requires a lot of effort and occurs at high costs. In addition, it results in reduced efficiency of recombinant protein production. Therefore, the development of an improved baculovirus-insect cell technology allowing high expression of heterologous proteins while eliminating baculovirus BV and ODV production is highly desirable, and is the topic of this patent application. Such a baculovirus virion-free production system would represent a significant improvement over existing systems for the production of all kinds of biopharmaceuticals in insect cells.

[0012] The present invention is based on the identification of efficient baculovirus-insect cell based methods for producing biopharmaceuticals with reduced amounts or absence of baculovirus virions.

[0013] An object of the present invention thus provides a method for the production of a biopharmaceutical product, comprising:

[0014] (a) infecting a biopharmaceutical-producing insect cell with at least one baculovirus, said at least one baculovirus comprising a genome coding for said biopharmaceutical product, and

[0015] (b) maintaining the biopharmaceutical-producing insect cell under conditions such that the biopharmaceutical product is produced, wherein each genome of said at least one baculovirus is deficient for at least one gene essential for proper baculovirus virion assembly or wherein said biopharmaceutical-producing insect cell comprises an expression control system allowing the inactivation of at least one gene essential for proper baculovirus virion assembly.

[0016] In an embodiment, the invention relates to the above method, wherein said at least one gene essential for proper baculovirus virion assembly is made deficient in said genome by mutation, for example by way of nucleotide substitution, insertion or deletion.

[0017] In another embodiment, the invention relates to the above method, wherein the biopharmaceutical-producing insect cell is a recombinant insect cell comprising a construct expressing a dsRNA specific for the at least one gene essential for proper baculovirus virion assembly, the dsRNA being optionally expressed under the control of an inducible promoter.

[0018] In a further embodiment, the invention relates to the above method, wherein the at least one baculovirus is produced before step (a) in a baculovirus-producing cell expressing a complementing copy of the at least one gene essential for proper baculovirus virion assembly.

[0019] In yet another embodiment, the invention relates to the above method, wherein the at least one gene essential for proper baculovirus virion assembly is selected from vp80, vp39, vp1054 and p6.9.

[0020] In another embodiment, the invention relates to the above method, wherein the deficiency or inactivation of the at least one gene essential for proper baculovirus virion assembly does not affect very late gene expression from said baculovirus in comparison to very late gene expression from the wild-type baculovirus vector.

[0021] In yet another embodiment, the invention relates to the above method, wherein the at least one baculovirus is preferably derived from AcMNPV or Bombyx mori (Bm) NPV.

[0022] In a further embodiment, the invention relates to the above method, wherein the biopharmaceutical product is a recombinant protein, a recombinant virus, a virus-derived vector, or a virus-like particle.

[0023] In another embodiment, the invention relates to the above method, wherein the biopharmaceutical product is a recombinant AAV vector. Furthermore, the invention relates to the above method, wherein the biopharmaceutical product is a vaccine. Representative examples of vaccines than can be produced with the method of the present invention include, but are not limited to, influenza virus-like particles or influenza subunit vaccines, and vaccines against Human papillomavirus.

[0024] In a further embodiment, the invention relates to the above method, wherein the biopharmaceutical product is coded by at least one gene introduced in the recombinant baculovirus genome under the control of a baculovirus promoter, preferably the p10 or polyhedrin promoter.

[0025] Another object of the invention provides the use of a baculovirus-insect cell system for the production of a biopharmaceutical product wherein the baculovirus-insect cell system comprises a biopharmaceutical-producing insect cell infected with at least one recombinant baculovirus, wherein:

[0026] the, or each, recombinant baculovirus comprises a recombinant baculovirus genome that encodes the biopharmaceutical product, or at least one component of the biopharmaceutical product, and

[0027] the recombinant baculovirus genome is deficient for at least one gene essential for proper assembly of said baculovirus, or the biopharmaceutical-producing insect cell comprises an expression control system allowing the inactivation of the at least one gene essential for proper baculovirus virion assembly.

[0028] Yet another object of the invention relates to a bacmid comprising a baculovirus genome, wherein said genome is deficient for a gene essential for proper baculovirus virion assembly, preferably wherein the genome of said baculovirus is deficient for vp80, vp39, p6.9 or vp1054. In a particular aspect, said bacmid is derived from AcMNPV and is lacking the vp80 ORF.

[0029] A further object of the invention relates to a recombinant AcMNPV baculovirus vector, wherein the genome of said baculovirus is deficient for a gene essential for proper baculovirus virion assembly, preferably wherein the genome of said baculovirus is deficient for vp80, vp39, vp1054 or p6.9. In a particular aspect, the invention relates to a recombinant AcMNPV baculovirus lacking the vp80 ORF.

[0030] The invention has also as an object an insect cell infected with the above mentioned recombinant AcMNPV baculovirus.

[0031] Another object of the invention relates to an insect cell, comprising a construct expressing a dsRNA specific for a gene essential for proper baculovirus virion assembly, preferably directed against vp80, vp39, vp1054 and/or p6.9, said construct being preferably integrated in the genome of the insect cell.

[0032] A further object of the invention relates to an insect cell comprising an expression cassette coding for a gene essential for proper baculovirus virion assembly. In particular, the invention relates to said insect cell, wherein the gene coded by the expression cassette is vp80, vp39, vp1054 and/or p6.9.

[0033] Another object of the invention relates to a method for the production of a baculovirus deficient for at least one gene essential for proper baculovirus virion assembly, comprising the step of transfecting an insect cell comprising an expression cassette coding for a gene essential for proper baculovirus virion assembly, with a bacmid comprising a baculoviral genome, wherein said genome is deficient for a gene essential for proper baculovirus virion assembly, preferably wherein the genome of said baculovirus is deficient for vp80, vp39, p6.9 and/or vp1054, wherein the gene essential for proper baculovirus virion assembly deficient in said bacmid is the gene coded by the expression cassette comprised in said insect cell.

[0034] The present invention relates to the production of biopharmaceuticals in insect cells by implementing a baculoviral system, but without coproduction of contaminating baculovirus virions. The methods of the invention simplify the downstream processing of biopharmaceuticals produced in insect cells to a large extent.

[0035] Thus, the invention relates to methods for the production of a biopharmaceutical product implementing a baculoviral system designed to avoid the production of contaminating baculoviral virions. The method of the present invention comprises the infection of biopharmaceutical-producing insect cells with at least one baculovirus coding for said biopharmaceutical product.

[0036] Baculoviruses are enveloped DNA viruses of arthropods, two members of which are well known expression vectors for producing recombinant proteins in cell cultures. Baculoviruses have circular double-stranded genomes (80-200 kbp) which can be engineered to allow the delivery of large genomic content to specific cells. The viruses used as a vector are generally Autographa californica multicapsid nucleopolyhedrovirus (AcMNPV) or Bombyx mori (Bm)NPV (Kato et al., 2010).

[0037] Baculoviruses are commonly used for the infection of insect cells for the expression of recombinant proteins. In particular, expression of heterologous genes in insects can be accomplished as described in for instance U.S. Pat. No. 4,745,051; Friesen et al (1986); EP 127,839; EP 155,476; Vlak et al (1988); Miller et al (1988); Carbonell et al (1988); Maeda et al (1985); Lebacq-Verheyden et al (1988); Smith et al (1985); Miyajima et al (1987); and Martin et al (1988). Numerous baculovirus strains and variants and corresponding permissive insect host cells that can be used for protein production are described in Luckow et al (1988), Miller et al (1986); Maeda et al (1985) and McKenna (1989).

[0038] According to the present invention, any genome derived from a baculovirus commonly used for the recombinant expression of proteins and biopharmaceutical products may be used. For example, the baculovirus genome may be derived from for instance AcMNPV, BmNPV, Helicoverpa armigera (HearNPV) or Spodoptera exigua MNPV, preferably from AcMNPV or BmNPV. In particular, the baculovirus genome may be derived from the AcMNPV clone C6 (genomic sequence: Genbank accession no. NC_001623.1--SEQ ID NO:1).

[0039] The terms "Biopharmaceutical", "Biopharmaceuticals" and "Biopharmaceutical Product" are intended to define medical drugs produced using biotechnology. As such, biopharmaceuticals may correspond to recombinantly produced drugs such as recombinant proteins, notably recombinant hormones or recombinant proteins for use as vaccines, viruses, for example therapeutic recombinant AAV or other viral vectors for use in gene therapy, as well as virus-like particles (or VLPs). Such biopharmaceuticals are intended to be administered to a subject in need thereof for the prophylactic or curative treatment of a disease condition in said subject which may be of either human or animal origin.

[0040] A biopharmaceutical product may correspond to a single chain protein or peptide, for example in the case of a therapeutic recombinant protein, or may be a complex structure such as a virus or a virus-like particle. In the latter two cases, the components of the complex may be expressed from several recombinant baculoviruses, each carrying at least one component of the complex structure, or from a single baculovirus whose genome has been genetically modified by the insertion of sequences encoding all the components of the complex. For example, for the production of a recombinant AAV, a system comprising three baculoviruses may be used: a baculovirus coding for the AAV Rep proteins, a baculovirus coding the AAV Cap proteins and a baculovirus coding the AAV-ITR genome comprising a therapeutic gene between the two AAV ITRs. A system comprising two baculoviruses is also available now, for which the DNA sequences coding for the AAV Rep proteins and the AAV Cap proteins are provided by one baculovirus.

[0041] In a preferred embodiment of the invention, the heterologous gene(s) encoding the biopharmaceuticals are placed under the control of a baculoviral promoter. For example, the heterologous gene(s) is (are) placed under the control of the polyhedrin or p10 promoter, or of any other baculoviral promoter commonly used for expression in an insect cell (e.g. ie-1, p6.9, gp64 or the Orchyia pseudotsugata (Op) MNPV ie-2 promoter). In a preferred embodiment of the invention, the baculoviral promoter is selected from very late expression promoters, for example from the p10 and polyhedrin promoters, preferably under the control of the polyhedrin promoter.

[0042] In the method of the present invention, at least one gene essential for proper baculovirus virion assembly is either absent from the genome of the recombinant baculovirus(es) implemented in the above described method, or its expression is prevented. The inventors have shown that the deletion or inactivation of such genes results in the reduction, or even the complete absence, of budded virions and/or occlusion derived virions, the two forms of a baculovirus.

[0043] A "gene essential for proper baculovirus virion assembly" is a gene whose deficiency or inactivation in a baculovirus-producing cell negatively impacts the number of BVs and ODVs produced from said cell. Such a gene may be identified as provided in the herein below examples. In particular, one can use double stranded RNAs specific for a particular baculoviral gene to assess the impact of the absence of said particular gene on the production of BVs and ODVs, for example by detecting the expression of a reporter gene present in the baculoviral genome in the cell culture, and thus determine the spreading or absence of spreading of the baculovirus (single-infection phenotype). Alternatively baculovirus virions may be detected by the presence of baculoviral structural proteins or genome sequences in the culture medium when sampling for BV production. Both virion types may be detected by electron microscopy.

[0044] In a preferred embodiment of the invention, the gene essential for proper baculovirus virion assembly is selected from vp80, vp39, vp1054 and p6.9. More preferably, the gene is selected from vp80 and vp39, said gene being preferably vp80.

[0045] The invention provides the inactivation of genes essential for proper baculovirus virion assembly. Several strategies may be implemented for this purpose, and in particular: the mutation, for example by deletion, of the selected gene(s) in the recombinant baculovirus genome; or the reduction of the expression of the selected gene by an expression control system provided in the biopharmaceutical-producing insect cell intended to be infected by the baculovirus. Preferably, the expression control system involves the down-regulation by RNA interference of the expression of the protein(s) encoded by the selected gene(s).

[0046] In one embodiment of the invention, the genome of the at least one baculovirus implemented in the method of the invention is deficient for at least one gene essential for proper baculovirus virion assembly, in particular for a gene coding for vp80, vp39, vp1054 and/or p6.9, preferably for vp80 and/or vp39, and even more preferably for vp80. More particularly, said genome is derived from AcMNPV, more particularly from AcMNPV clone C6 genome sequence (Genbank accession no. NC_001623.1--SEQ ID NO: 1). Accordingly, in one aspect the invention provides the method as defined above, wherein the baculoviral genome is an AcMNPV genome, in particular an AcMNPV clone C6 genome, deficient for the gene coding for vp80, vp39, vp1054 and/or p6.9, preferably for vp80 and/or vp39, and even more preferably for vp80. As is well known in the art and specified in Genbank accession no. NC_001623.1, these genes are positioned as follows in AcMNPV clone C6 genome (i.e. in SEQ ID NO:1): positions 89564-91639 for vp80; positions 75534-76577 for vp39 (complementary sequence); positions 45222-46319 for vp1054; positions 86712-86879 for p6.9 (complementary sequence).

[0047] It should be noted that in case the biopharmaceutical product is a complex product comprising various subunits each encoded by different baculoviruses, the genomes of all the implemented recombinant baculoviruses are deficient for the selected essential gene, so as to avoid complementation of one genome by another. In other words, when several baculoviruses are used to infect the same biopharmaceutical-producing insect cell, each of these baculoviruses are deficient for the same gene(s) essential for proper baculovirus virion assembly.

[0048] According to the present invention, a gene may be made deficient by mutating said gene. A mutation of a gene essential for proper baculovirus virion assembly is a modification of said gene that results in the complete absence of a functional essential gene product. Accordingly, said mutation may result in the introduction of one or several stop codons in the open reading frame of the mRNA transcribed from the gene essential for proper baculoviral virion assembly or may correspond to the deletion, either total or partial, of the gene essential for proper baculovirus virion assembly. A gene essential for proper baculoviral virion assembly may be mutated by way of nucleotide substitution, insertion or deletion in the sequence of all or a part of the wild type gene (for example in the sequence provided in Genbank Accession No. NC_001623.1, for a genome derived from AcMNPV). The mutation may correspond to the complete deletion of the gene, or to only a part of said gene. For example, one may delete at least 50%, more preferably at least 60%, more preferably at least 70%, more preferably at least 80% and even more preferably at least 90% of the gene essential for proper baculoviral virion assembly.

[0049] The mutant baculoviral genome may be produced using standard methods well known in the art, such as site-directed mutagenesis (see, e.g., Sambrook et al. (1989)) and Lambda red recombination (Datsenko & Wanner, 2000). The gene essential for proper baculovirus virion assembly may in particular be deleted as provided in the below examples. In summary, one can make use of the mutant LoxP sites described by Suzuki at al. (2005), by replacing either totally or in part the gene essential for proper baculovirus virion assembly with a reporter gene flanked by mutant LoxP sites by recombination. The reporter gene (for example the gene coding for chloramphenicol acetyl transferase (cat) is then excised by implementing a recombination with Cre recombinase.

[0050] This embodiment is illustrated in the below examples and is detailed for baculoviruses whose genome has been modified by deleting a 2074-bp fragment of the vp80 ORF in the AcMNPV genome. This particular genome is part of the present invention, but is given as a non limiting example of what is a mutant baculoviral genome according to the invention.

[0051] It should be noted that recombinant engineering of the baculovirus genome may result in the insertion of several sequences like cloning sites or recombination sites (for example one remaining LoxP site after recombination with Cre recombinase). This is irrelevant as long as the resulting genome is made deficient for the selected gene essential for proper baculovirus virion assembly.

[0052] In this embodiment, wherein the genome of the at least one baculovirus is deficient for at least one gene essential for proper assembly of baculovirus virion, the production of recombinant budded baculovirus particles needed for the initial infection of the cells producing the bio-pharmaceuticals requires the implementation of special cells rescuing the deficient gene, i.e. these baculovirus-producing cells express the selected gene. In other terms, the baculovirus-producing cell expresses a complementing copy of the at least one gene essential for proper baculoviral virion assembly which is deficient in the baculovirus genome. For example, a Sf9-derived cell line constitutively producing the product of the gene essential for proper assembly of the baculovirus virion may be established. This recombinant cell line is used for production of baculovirus seed stock while conventional insect cell lines like Sf9, Sf21 or High-five cell lines can be infected with the produced baculovirus for heterologous expression of the biopharmaceutical product. Accordingly, the invention also relates to an insect cell modified so as to express a gene essential for proper baculovirus assembly, said gene being mutated in a baculovirus used for the production of biopharmaceuticals, as defined above. Such a cell line used for the production of the mutant baculovirus vector implemented in the method of the present invention is referred to as a "baculovirus-producing cell". When the baculovirus genome is deficient for a gene essential for proper baculovirus virion assembly, the baculovirus-producing insect cell must provide and express said gene in order to complement the deficiency and to produce an infectious baculovirus. In a particular embodiment, the insect cell used for the production of the baculovirus is modified by transfection with an expression cassette coding for at least one gene essential for proper baculovirus virion assembly. In an embodiment, said expression cassette is integrated in the genome of said cell. One may also use insect cells transiently transfected with at least one plasmid comprising the expression cassette. The term "expression cassette" denotes a construct comprising the coding sequence of a gene of interest functionally linked to expression control sequences. Such an expression cassette may be a plasmid comprising the ORF of a gene essential for proper baculovirus virion assembly placed under the control of a promoter functional in the selected insect cell, and does not contain baculoviral genome sequences other than the gene essential for proper baculovirus virion assembly to be complemented and optionally the promoter sequence allowing the expression of said gene (in particular, an expression cassette is not a bacmid or any other baculoviral entire genome). Exemplary expression control sequences may be chosen among promoters, enhancers, insulators, etc. In one embodiment, the complementing gene is derived from the genome of the baculovirus in which the gene essential for proper baculovirus virion assembly has been made deficient. In another embodiment, the complementing gene originates from the genome of a different baculovirus species than the baculovirus genome used for the production of biopharmaceuticals. For example, the baculovirus used for the production of biopharmaceuticals may be derived from the AcMNPV genome, and the complementing gene introduced in the baculovirus-producing cell is derived from BmNPV or SeMNPV. More specifically, the baculovirus genome may be made deficient for vp80, vp39, vp1054 and/or p6.9 and the baculovirus-producing cell may comprise a copy of a gene from BmNPV or SeMNPV able to complement these genes (e.g. as provided in the examples, p6.9 is deleted in the AcMNPV genome and the baculovirus-producing cell provides a rescuing copy of the SeMNPV p6.9 gene).

[0053] The invention thus also provides a method for the production of a baculovirus deficient for at least one gene essential for proper baculovirus virion assembly, comprising the step of transfecting an insect cell comprising an expression cassette coding for a gene essential for proper baculovirus virion assembly, with a bacmid comprising a baculoviral genome, wherein said genome is deficient for a gene essential for proper baculovirus virion assembly, preferably wherein the genome of said baculovirus is deficient for vp80 or vp39, p6.9 and/or vp1054, wherein the gene essential for proper baculovirus virion assembly deficient in said bacmid is the gene coded by the expression cassette comprised in said insect cell. According to this method, the gene deficient in the baculoviral genome is complemented by the gene expressed in the insect cell. The cells transfected with the bacmid are maintained in conditions such that baculovirus virions are produced. These produced baculovirus virions, which comprise a genome where at least one gene essential for proper baculovirus virion assembly is lacking, are then collected for their subsequent use for infecting biopharmaceutical-producing insect cells for the production of the biopharmaceutical.

[0054] In the embodiment where the genome of the baculovirus is deficient for at least one gene essential for baculovirus virion assembly, the biopharmaceutical-producing insect cell must be unable to complement the deficiency of said gene. Otherwise, the deficiency would be rescued by the biopharmaceutical-producing cell and BVs and ODVs might be produced. The presence or absence of a gene essential for proper baculovirus assembly may be monitored for example by checking said cell by a PCR specific to said gene or by detection of the protein product of this gene (for example by western-blot with an antibody specific to said gene product). Cells expressing a functional product of the gene essential for proper baculovirus virion assembly which has been made deficient in the genome of the implemented baculovirus intended to infect said cell must be disregarded as bio-pharmaceutical producing cells.

[0055] In another embodiment of the invention, the expression of the gene essential for proper assembly of baculovirus virions is controlled by an expression control system. The term "expression control system" defines a modification of the baculovirus-producing insect cell system/the biopharmaceutical-producing cell system and/or yet another adaptation of the viral genome, resulting in the specific regulation of the gene essential for proper baculovirus virion assembly. This system may be an inducible expression system (for example Tet-On, Tet-Off, ecdysone-based systems (Dai et al., 2005) or baculovirus homologous region (hr) containing elements, such as the hr2 system described by Aslanidi et al. (2009), allowing the desired triggering or shutdown of the essential gene, an RNA interference expressing construct or a combination of these.

[0056] In a particular embodiment, the expression of the gene essential for proper assembly of baculovirus is inactivated by RNA mediated silencing, or RNA interference (Salem & Maruniak, 2007, Kanginakudru et al., 2007). Preferably, an insect-cell derived cell line, in particular a Sf9-derived cell line, is established by stably transforming such a cell with a construct coding for a gene-specific double stranded RNA (dsRNA) to silence the expression of the gene essential for proper baculovirus virion assembly. This dsRNA expressing cell line is used for the expression of the biopharmaceutical product after infection with the recombinant baculovirus(es) carrying the gene coding for said biopharmaceutical product. In this embodiment, seed stock recombinant baculovirus(es) may be produced with conventional Sf9, Sf21 or High-Five cell lines (i.e. without the need of a complementing copy of the gene in the cell), since in this case the baculovirus genome comprises the wild-type gene essential for proper baculovirus virion assembly.

[0057] In yet another embodiment of the invention, the gene essential for proper baculovirus virion assembly is placed under the control of an inducible promoter, allowing either the expression or repression of said gene under controlled conditions.

[0058] In a preferred embodiment, the number of baculovirus virions produced in the method of the present invention is reduced by at least 50% in comparison to the number of baculovirus otherwise produced by the biopharmaceutical-producing cell using a baculovirus genome comprising all the genes essential for proper baculovirus virion assembly. More preferably, the number of baculovirus virions is reduced by at least 60%, at least 70%, at least 80%, at least 90% and most preferably by at least 95% in comparison to a wild type baculovirus genome.

[0059] As discussed above, the use of insect cell/baculovirus systems for the production of biopharmaceuticals in the prior art is characterized by the co-production of huge quantities of recombinant baculoviruses (and may be over 10.sup.8 pfu/ml) in parallel to the biopharmaceutical product, needing carefully developed and optimized downstream processing protocols to inactivate and eliminate this baculovirus contamination. Inactivation can be performed by the addition of a detergent step leading to disintegration of the lipid layer of the contaminating baculovirus, such as used for the purification of virus-like particles for vaccine purposes (porcine parvovirus-VLPs (Maranga et al. (2002)) or rotavirus-VLPs (Mellado et al. (2008)) or the purification of different serotypes of AAV (Smith et al. 2009).

[0060] Further efficient separation steps have been used: centrifugation (Wang et al. (2000); Maranga et al. (2002); Mellado et al. (2008)), microfiltration (Tellez (2005)), negative elimination of baculovirus proteins (e.g. Mellado et al. (2008)) or positive affinity chromatography (retention/capture of a biopharmaceutical--flow through of the contaminating proteins, such as capture of the vp7 protein of rotavirus by Concanavalin A chromatography (Mellado et al. (2008)), capture of the immunogenic chimeric rVP2H infectious bursal disease virus particles by immobilized metal-ion affinity chromatography (Wang et al. (2000)) or capture of different AAV serotypes by immunoaffinity chromatography using camelid antibodies (Smith et al. 2009). In particular, due to the use of highly specific immunoligands, the use of immunoaffinity allows the complete separation of the to be purified biopharmaceutical (e.g. specific AAV) from any contaminant, and in the case of the baculovirus system, from the huge contamination by baculovirus due to the concomitant production of baculovirus in parallel to the biopharmaceutical.

[0061] These references present very clearly the need of these different process steps for inactivating and eliminating residual baculovirus contaminants, because without these steps, the biopharmaceutical product is still considerably contaminated by various baculovirus proteins and cannot be used for clinical purposes.

[0062] The method of the present invention allows a significant reduction of the number of contaminating baculovirus virions, or even a complete absence. As a consequence, a reduced number of purification steps will be necessary for getting a biopharmaceutical for clinical purposes (or even no purification step if no baculoviral virion is produced). Thus, the biopharmaceutical production and purification protocol is simplified because by using the method of the present invention, the need for eliminating residual baculovirus virion is greatly reduced. In case a simplified purification protocol is still to be applied, the skilled artisan may select at least one of the above identified methods and protocols to obtain a purified biopharmaceutical product.

[0063] Preferably, the selected essential gene is a gene whose inactivation does not affect baculoviral very late gene expression, compared to the original baculovirus vector. In the AcMNPV genome (and other alpha-baculoviruses), the p10 and polyhedrin promoters are the very late expression promoters and it should be noted that in baculovirus/insect cell production systems, the heterologous gene is most commonly inserted under the control of these very strong promoters allowing expression of very large amounts of recombinant proteins. The inactivation of a gene essential for proper baculovirus virion assembly, which does not affect very late gene expression is thus preferred. The term "does not affect very late gene expression" denotes the fact that the level of recombinant protein expression from very late baculovirus promoter comprised in the genome of a baculovirus modified according to the invention is at least 70% in comparison to the levels obtained from a non-modified genome, more preferably greater than 80%, more preferably greater than 90%. It should be mentioned that the level of expression of a biopharmaceutical product from a very late baculoviral promoter may even be greater than 100% of the level obtained with the non-modified vector in the method of the present invention.

[0064] Among the genes tested by the inventors, the vp80 gene is particularly preferred since its deletion does not affect very late expression, while it totally prevents production of BVs and results in a significant reduction in the number of intracellular nucleocapsids, the precursors of ODVs.

[0065] Very late expression may be evaluated by placing a reporter gene, for example a gene coding for a GFP, in particular egfp, or a luciferase gene, under the control of the polyhedrin or p10 promoter in a wild type AcMNPV vector and in a mutant AcMNPV genome from which the essential gene has been inactivated, and by comparing the expression of the product of the reporter gene from both genomes. Preferably, very late expression from the vector with a mutated baculovirus backbone is at least 60% of the expression level obtained with the wild type AcMNPV vector and preferably higher than 80%, more preferably higher than 90%, as measured from a reporter gene under the control of either p10 or polyhedrin gene promoters.

[0066] The invention also relates to a method for screening baculoviral genes, the inactivation of which could be useful for producing biopharmaceuticals without contaminating baculovirus virions in an insect cell--baculovirus system as defined above, comprising:

[0067] a) providing a cell culture of cells containing a baculoviral genome;

[0068] b) contacting said cell culture with means for inactivating at least one test baculoviral gene of said baculoviral genome, for example with RNA interference; and

[0069] c) testing virion formation from said cell culture in comparison to virion formation from a cell culture not contacted with said means;

wherein a test gene is selected as potentially useful for producing biopharmaceuticals if its inactivation results in a reduction of baculoviral virion formation.

[0070] In a particular embodiment, the method for screening of the invention further comprises step d) of testing very late gene expression from the cell culture contacted with said means in comparison to very late gene expression from a cell culture not contacted with said means;

[0071] wherein a test gene is selected as potentially useful for producing biopharmaceuticals if its inactivation results in a reduction of baculoviral virion formation and if it does not affect very late gene expression from said baculoviral genome.

[0072] The invention also relates to a method for screening baculoviral genes, the inactivation of which could be useful for producing biopharmaceuticals without contaminating baculovirus virions in an insect cell--baculovirus system as defined above, comprising:

[0073] inactivating at least one test gene of a baculoviral genome (for example by deletion of said test gene in said genome);

[0074] evaluating baculoviral very late gene expression from said baculoviral genome as defined above;

[0075] determining production of baculoviral virions from cells containing said baculoviral genome; wherein a gene is selected as potentially useful for the production of biopharmaceuticals if its inactivation

[0076] results in a reduction in the production of baculoviral virions, and

[0077] does not affect very late gene expression from said baculoviral genome, as defined above.

[0078] In a particular embodiment of the method for screening a baculoviral gene, the inactivation of which could be useful for producing biopharmaceuticals, the inactivation of the test gene is carried out with dsRNA specific for said test gene. In particular, the candidate baculovirus gene can be identified by knocking down its expression by RNA interference to test its role in virion formation.

[0079] The invention will now be illustrated with the following examples, which are provided as non limiting exemplary embodiments of the invention.

LEGENDS TO THE FIGURES

[0080] The patent or application file contains at least one drawing executed in color. Copies of this patent or patent application publication, with color drawing(s), will be provided by the Office upon request and payment of the necessary fee.

[0081] FIGS. 1A-1D. dsRNA-mediated gene silencing screening. Insect Sf9 cells were seeded in 24-well tissue culture plates (2.times.10.sup.5 cells/well) in 1 ml Sf-900 II SFM culture medium at 28.degree. C. After two hours, the culture medium was removed, and the cells were infected with recombinant baculovirus carrying the egfp gene under control of the polyhedrin promoter (AcMNPV-EGFP) under standard conditions.

[0082] (A) Determination of very late gene expression level using fluorescent microscopy. Cells were infected at MOI=10 TCID.sub.50 units/cell and transfection with gene-specific dsRNA for vp1054, vp39, vp80, dbp and ec-27 was performed at 1 h post infection (p.i.). The level of very late gene expression was checked by EGFP-specific fluorescence at 48 h p.i. dsRNAs specific for egfp and cat sequences were used as RNAi controls. (B) Measurement of very late gene expression levels by an immunoblotting-based assay. The cells were infected with AcMNPV-EGFP at MOI=1 and transfection with gene-specific dsRNA was also performed at 1 h p.i. The level of very late gene expression was analyzed by using a rabbit anti-EGFP polyclonal antiserum at 48 h p.i. Anti-vp39 and anti-.alpha.-tubulin antibodies were used as internal controls. (C) Titration and detection of produced budded virions in dsRNA-treated cells. Budded virions were harvested at 36 hours p.i., and used either for end-point dilution assays to measure titers of infectious virions, or for PCR-based detection to check the presence of virus particles. (D) Presence of occlusion-derived virions and rod-shaped structures in vp39- and vp80-down-regulated cells. The cells were harvested 36 hours p.i., lysed, and the cell lysates were ultracentrifuged through a cushion of 40% sucrose solution (45,000 rpm for 1 hour, Beckman SW55). Pellets were resuspended in demi-water and analyzed by negative staining electron microscopy. The bars represent 100 nm.

[0083] FIGS. 2A-2B. Construction of the AcMNPV vp80-null bacmid. (A) Strategy for construction of a vp80-null bacmid containing a complete deletion of the AcMNPV vp80 open-reading frame via homologous recombination in E. coli. At the first step, a 2074-bp fragment encompassing the vp80 ORF was deleted and replaced with a sequence cassette containing the chloramphenicol (cat) resistance gene flanked by modified loxP (LE and RE) sites. Subsequently, the antibiotic resistance gene (cat) was eliminated from the bacmid sequence using the Cre/loxP recombination system. The promoter sequence of the p48 gene and the polyadenylation signal of the he65 gene remained intact. Oligonucleotide pairs were used in PCR analysis of the wild-type locus and two vp80 knock-out genotypes to confirm the deletion of the vp80 ORF and the correct insertion/deletion of the chloramphenicol resistance gene cassette, as indicated by unilateral arrows. Their names are designated according to nucleotide sequence coordinates. Primers for cat gene cassette amplification are named cat-F and cat-R. (B) PCR-based detection of the presence or absence of sequence modifications in the vp80 locus in the original AcMNPV bacmid (Ac-wt), Ac-vp80null(+cat), and Ac-vp80null(-cat) bacmids. The top figure confirms the vp80 gene deletion and the insertion of the cat cassette into the vp80 locus with primer pairs 90292/90889 and cat-F/cat-R. The bottom figure shows PCR-based verification of the correct recombination processes in the vp80 locus using the 89507/91713 primer pair.

[0084] FIGS. 3A-3C. Viral replication capacity of AcMNPV-vp80 knockout and repaired bacmid constructs using transfection-infection assays. (A) Schematic representation of expression cassettes transposed into the polyhedrin locus. Four repair constructs were made (vp80 driven by its native promoter, vp80 driven by the polyhedrin promoter, N-terminally FLAG-tagged vp80 and C-terminally FLAG-tagged vp80, both expressed from its native promoter). The bacmid genome backbones used for transfection assays are indicated on the left. As positive control of viral replication the wild type AcMNPV (bMON14272) bacmid was used. The Ac-gp64null bacmid was used as negative control representing a prototype bacmid with a "single-cell infection" phenotype. (B) Time course fluorescence microscopy showing the propagation of the infection in Sf9 cells transfected with indicated bacmid constructs. Progress of viral infection was checked by EGFP detection at indicated times post transfection. At 120 hours p.t., the cell culture supernatants were collected to initiate a secondary infection. (C) Secondary infection assay. EGFP was detected at 72 hours p. i. to signal the progress of infection.

[0085] FIGS. 4a-4d. Growth curves of AcMNPV-vp80null repaired bacmid constructs generated from transfection time-course assays. Sf9 cells were transfected with 5.0 .mu.g of DNA from each repair bacmid. (a) vp80 driven by its native promoter, (b) vp80 driven by the polyhedrin promoter, (c) N-terminally FLAG-tagged vp80, and (d) C-terminally FLAG-tagged vp80, both expressed from the vp80 promoter. Cell culture supernatants were harvested at the indicated time points post-transfection and analysed for the production of infectious budded virus by a TCID.sub.50 end-point dilution assay. Infectivity was determined by monitoring EGFP expression. The points indicate the averages of titers derived from three independent transfections, and the error bars represent the standard deviation.

[0086] FIGS. 5A-5B. The AcMNPV-vp80null mutant is unable to produce any infectious/non-infectious budded virions. The Sf9 cells were independently transfected with 20 .mu.g of bacmid DNA of Ac-.DELTA.vp80 (a), Ac-wt (b), Ac-.DELTA.vp80-vp80 (c), Ac-.DELTA.vp80-pH-vp80 (d), Ac-.DELTA.vp80-FLAG-vp80 (e), or Ac-.DELTA.vp80-vp80-FLAG (f). Five days p.t., the budded virus-enriched cell culture supernatants were ultracentrifuged and budded viruses were observed by negative staining electron microscopy (A). The bars represent 200 nm. Parallelly, harvested budded virions were also either separated on SDS-PAGE, blotted and immuno-detected using anti-VP39 antibody or used for PCR-based detection to detect the presence of viral particles (B).

[0087] FIGS. 6A-6H. The null bacmid mutant in the vp80 gene forms small numbers of nucleocapsids, and is deficient in production of occlusion-derived virions. The Sf9 cells transfected either with Ac-.DELTA.vp80 (A to D), Ac-.DELTA.vp80-vp80 (E, F), or Ac-wt (G, H) were fixed, stained, embedded and thin-sectioned as described in Materials and Methods. (A) Representative overview of Sf9 cell transfected with Ac-vp80null bacmid mutant. (B) The Ac-vp80null mutant does form lower numbers of nucleocapsids in the virogenic stroma (C), and no occlusion-derived virions in the ring zone of transfected cells (D). On the other hand, repair bacmid construct Ac-.DELTA.vp80-vp80 fully regenerates formation of plenty of nucleocapsids in the virogenic stroma (E), as well as normally-appearing occlusion-derived virions in the ring zone of transfected cells (F). Representative images of the virogenic stroma (G) and the ring zone (H) of cells transfected with Ac-wt bacmid. Bars represent 500 nm. Abbreviations: Nc, nucleocapsid; NM, nuclear membrane; Nu, nucleus; RZ, ring zone; Mi, mitochondrion; ODV, occlusion-derived virions; VS, virogenic stroma.

[0088] FIGS. 7A-7B. Functional complementation of the Ac-vp80null bacmid mutant using the trans-acting vp80 gene. The Sf9 cells were transfected with either pIZ-flag-vp80 (A) or pIZ (B) vector, and subjected to Zeocin-based selection. Three weeks post-transfection, polyclonal Zeocin resistant populations of cells were seeded to a new 6-well plate and transfected with the Ac-vp80null bacmid mutant to check complementation activity. Virus propagation was monitored by EGFP-specific fluorescence at 72 h and 96 h p.t. At 120 hours p.t., the cell culture supernatants were collected to initiate a secondary infection in untreated (wild-type) Sf9 cells (right panel). EGFP was detected at 72 hours p.i. to signal the progress of infection. EGFP was detected at 120 hours p.i. to signal the progress of infection.

[0089] FIGS. 8A-8B. Construction of an AcMNPV vp39-null bacmid. (A) Strategy for construction of a vp39-null bacmid containing a partial deletion of the AcMNPV vp39 open-reading frame via homologous recombination in E. coli. At the first step, an internal 498-bp fragment of the vp39 ORF was deleted and replaced with a sequence cassette containing the chloramphenicol (cat) resistance gene flanked by modified loxP (LE and RE) sites. Subsequently, the cat gene was eliminated from the bacmid sequence using the Cre/loxP recombination system. The promoter sequences of the lef-4 and cg-30 genes were not affected. Arrows indicate the positions of oligonucleotide pairs used in PCR analysis of the wild-type locus and two vp39 knock-out genotypes to confirm the partial deletion of the vp39 ORF and the correct insertion/deletion of the cat gene cassette. Primers names are designated according to the nucleotide sequence coordinates. (B) PCR-based detection of the presence or absence of sequence modifications in the vp39 locus of Ac-wt, Ac-vp39null (+cat), and Ac-vp39null (-cat) bacmids. The figure shows the PCR-based verification of the correct recombination processes in the vp39 locus using the 75834/76420 primer pair.

[0090] FIGS. 9A-9C. Determination of viral replication capacity of AcMNPV-vp39 knockout and repaired bacmid constructs using transfection-infection assays. (A) Schematic representation of expression cassettes, Tn7-based transposed into the polyhedrin locus. (1) vp39 expressed from the polyhedrin promoter, (2) a double gene vp39 and lef-4, both driven by their native promoters, (3) a double gene vp39 and cg-30 both driven by the polyhedrin promoter, and finally (4) a double gene construct of N-terminally FLAG-tagged vp39 driven by the polyhedrin promoter and the cg-30 ORF expressed from both its native and also the more upstream polyhedrin promoter. The parental bacmid genome backbones used for transfection assays are indicated on the left. The wild type AcMNPV (bMON14272) bacmid was used as positive control of viral replication. (B) Time course fluorescence microscopy showing the propagation of the infection in Sf9 cells transfected with indicated bacmid constructs. Viral progressions were checked by EGFP detection at indicated times post transfection. At 168 hours p.t., the cell culture supernatants were collected to initiate a secondary infection. (C) Secondary infection assay. EGFP detection was performed at 72 hours p.i. to measure progress of the infection.

[0091] FIGS. 10A-10B. Construction of an AcMNPV vp1054-null bacmid. (A) Strategy for the construction of a vp1054-null bacmid containing a deletion of the AcMNPV vp1054 open-reading frame via homologous recombination in E. coli. A 955-bp sequence from the 3'-end of the vp1054 ORF was deleted and replaced with a cat sequence cassette flanked by modified loxP (LE and RE) sites. At the same time, a single point mutation was introduced to change the first translation codon ATG.fwdarw.Met to ACG.fwdarw.Thr, to prevent translation into a C-truncated VP1054 protein. It also meant that the internal AAT codon no. 32 of lef-10 was mutated to AAC, both encoding Asn. Subsequently, the cat gene was eliminated using the Cre/loxP recombination system. The promoter sequence of vp1054/lef-10 was not affected in the bacmid construct. Since the polyadenylation signal of the lef-10 gene was removed, a novel synthetic poly-A signal combined with stop codon (TAATAAA) was introduced at the 3'-end of the lef-10 ORF. Arrows represent locations of oligonucleotide pairs used in the PCR analysis of the wild-type locus and two vp1054 knock-out genotypes to confirm the deletion of the vp1054 ORF and correct insertion/deletion of the cat cassette. (B) PCR-based detection of the presence or absence of sequence modifications in the vp1054 locus of Ac-wt, Ac-vp1054null (+cat), and Ac-vp1054null (-cat) bacmids. The top figure is showing confirmation of the vp1054 gene deletion and insertion of the cat cassette into vp1054 locus using primer pairs 90292/90889 and cat-F/cat-R. The bottom figure shows CR-based verification of the correct recombination processes in the vp1054 locus using the 89507/91713 primer pair.

[0092] FIGS. 11A-11C. Viral replication capacity of AcMNPV-vp1054 knockout and repaired bacmid constructs using transfection-infection assays. (A) Schematic representation of expression cassettes transposed into the polyhedrin locus. The bacmid genome backbones used for transfection assays are indicated on the left. Two Ac-vp1054null-derived constructs were made: first construct carrying only egfp marker gene under control of p10 promoter, and second construct carrying both egfp marker and overlapping lef-10/vp1054 locus directed from their natural promoter sequences (d). As positive control of viral replication the wild type AcMNPV (bMON14272) bacmid was used (a). The Ac-gp64null bacmid was used as negative control representing a prototype bacmid with a "single-cell infection" phenotype (b). (B) Time course fluorescence microscopy showing the propagation of the infection in Sf9 cells transfected with indicated bacmid constructs. Progress of viral infection was checked by EGFP detection at indicated times post transfection. At 120 hours p.t., the cell culture supernatants were collected to initiate a secondary infection. (C) Secondary infection assay. EGFP was detected at 72 hours p.i. to signal the progress of infection.

[0093] FIGS. 12A-12B. Construction of an AcMNPV p6.9-null bacmid. (A) Strategy for construction of a p6.9-null bacmid containing a complete deletion of the AcMNPV p6.9 open-reading frame via homologous recombination in E. coli. A 164-bp fragment of the p6.9 ORF was deleted and replaced with a cat resistance gene flanked by modified loxP (LE and RE) sites. Subsequently, the cat gene was eliminated from the bacmid sequence using Cre/loxP recombination. The promoter sequence of p6.9 gene was left unaffected, since its sequence is overlapping with the p40 ORF. Arrows represent locations of primer pairs used in the PCR analysis of the wild-type locus and two p6.9 knock-out genotypes. (B) PCR-based detection of the presence or absence of sequence modifications in the p6.9 locus of Ac-wt, Ac-vp6.9null (+cat), and Ac-vp6.9null (-cat) bacmids. The top figure shows the insertion of the cat cassette into the p6.9 locus using primer pairs cat-F/cat-R. The bottom figure shows PCR-based verification of the correct recombination processes in the p6.9 locus using the 86596/86995 primer pair.

[0094] FIGS. 13A-130. Viral replication capacity of AcMNPV-p6.9 knockout and repaired bacmid constructs using transfection-infection assays. (A) Schematic representation of expression cassettes transposed into the polyhedrin locus. Two repair constructs were made (AcMNPV p6.9 and SeMNPV p6.9 genes, both driven by the AcMNPV p6.9 promoter). The bacmid genome backbones used for transfection assays are indicated on the left. As positive control of viral replication the wild type AcMNPV (bMON14272) bacmid was used. The Ac-gp64null bacmid was used as negative control representing a prototype bacmid with a "single-cell infection" phenotype. (B) Time course fluorescence microscopy showing the propagation of the infection in Sf9 cells transfected with indicated bacmid constructs. Progress of viral infection was checked by EGFP detection at indicated times post transfection. At 120 hours p.t., the cell culture supernatants were collected to initiate a secondary infection. (C) Secondary infection assay. EGFP was detected at 72 hours p.i. to signal the progress of infection. (D) Comparisons of growth curves of AcMNPV-p6.9null (a), AcMNPV-p6.9null rescued with AcMNPV p6.9 (b), and AcMNPV-p6.9null rescued with SeMNPV p6.9 (c) constructs with wild-type (Ac-wt) bacmid. Sf9 cells were transfected with 5.0 .mu.g of DNA from each bacmid, cell culture supernatants were harvested at the indicated time points post-transfection and analysed for the production of infectious budded virus by a TCID.sub.50 end-point dilution assay. Infectivity was determined by monitoring EGFP expression. The points indicate the averages of titers derived from three independent transfections, and the error bars represent the standard deviation.

[0095] FIGS. 14A-14B: Western blot analysis of Flag:vp80 in cells, BV and ODV. (A) Time course of vp80 expression in infected insect cells. Sf9 cells were infected with the Ac-.DELTA.vp80-Flag.vp80 repair virus, and harvested at indicated time points. Flag.VP80 was detectable by western blot analysis from 12 h to 72 h p.i. as a band of approximately 95 kDa. In addition, a second Flag.VP80-specific band of .about.80 kDa accumulated from 48 h until 72 h p.i. Tubulin was used as an internal loading control. (B) The VP80 associates with the nucleocapsid fraction of BV. Two days p.i., BVs were purified by isokinetic ultracentrifugation in a sucrose gradient and separated into nucleocapsid (Nc) and envelope (Env) fractions by Nonidet-P40-based extraction. Flag.VP80 was detected in the Nc fraction as a double-band with molecular weights between the two variants (80-kDa and 95-kDa) detected in infected Sf9 cells (upper panel). Correct separation into Nc and Env fractions was controlled by anti-VP39 and anti-GP64 antibodies (bottom panels). (C) VP80 is also a structural component of ODV-nucleocapsids. Sf9 cells were co-infected with Ac-.DELTA.vp80-Flag.vp80 (MOI=25) and AcMNPV strain E2 (MOI=5) viruses. Five days p.i., ODVs were released from occlusion bodies and subsequently separated into nucleocapsid (Nc) and envelope (Env) fractions. Western blot analysis showed that VP80 is present in the DV Nc fraction as a single band of .about.80 kDa. Proper fractionation into Nc and Env fractions was controlled using anti-PIF-1 antiserum (bottom panel).

[0096] FIGS. 15A-15C. Functional complementation of the Ac-vp80null bacmid defective in BV production by trans-complementation. (A) Detection of FLAG:VP80 in a transgenic Sf9-derived cell line (Sf9-vp80) by Western analysis. Tubulin was used as an internal loading control. (B) Time-course fluorescence microscopy (EGFP) to follow the infection in Sf9-vp80 cells transfected (i) or infected (ii) with the Ac-.DELTA.vp80 bacmid (a,b). At 120 h p.t., the cell culture supernatants were collected to initiate a secondary infection in either Sf9-vp80 (a) or Sf9 (b) cells (panels on the right side). As negative control Ac-.DELTA.vp80 was propagated in Sf9 cells (c), Ac-wt propagated in Sf9 cells (d) was used as positive control. (C) Comparative release of infectious BV virions. Sf9-vp80 cells were transfected with the Ac-.DELTA.vp80 bacmid and Sf9 cells with either the Ac-.DELTA.vp80 (negative control) or the Ac-wt (positive control) bacmid. BVs were quantified in cell culture supernatants at 6 days p.t. by end point dilution. Representative results of three independent assays with error bars giving the SD are shown.

[0097] FIGS. 16A-16C. Analysis of foreign gene expression by trans-complemented, replication-deficient baculovirus seed. Sf9 cells were infected with Ac-wt, Ac-.DELTA.vp80-Flag:vp80 or Ac-.DELTA.vp80 virus seed (MOI=10 TCID.sub.50 units per cell), all expressing egfp from the very late p10 promoter. (A) At 48 h p.i. the presence of EGFP, Flag:VP80 and GP64 was analyzed by Western blotting. Actin was used as an internal loading control. (B) Photomicrographs of cells expressing EGFP 72 h p.i. (top), and relative amount of EGFP measured by ELISA at 48 and 72 h p.i. (bottom) (C) Photomicrographs of cells expressing EGFP 72 h p.i. (top), and analysis of BV released to test for revertant genotypes by TCID.sub.50 titration (bottom). The results of three independent assays are shown with error bars (SD) (B and C).

[0098] FIGS. 17A-17D. The novel baculovirus-insect cell technology approach designated for the production of biopharmaceuticals free of contaminating baculoviral virions. (A) Insect cell engineering to express an essential viral factor (vp80) to complement a vp80 mutation in the virus. The transgenic Sf9 cells encode the vp80 ORF and a resistance gene allowing antibiotics-based selection of the transgenic cells. (B) Generation of an Ac-.DELTA.vp80 bacmid defective in production of BV and ODV virions. The bacmid lacks the entire vp80 ORF. (C) Production of a baculovirus seed stock by trans-complementation in the engineered Sf-vp80 cells. The Sf9-vp80 cells are transfected with the Ac-.DELTA.vp80 bacmid to produce trans-complemented virus progeny. After budded virus propagation, high-titer virus stocks are produced in the Sf9-vp80 packaging cells. (D) Baculovirus-based recombinant protein expression. Conventional Sf9 cells are infected with the trans-complemented budded virus progeny. Recombinant protein is expressed from very late baculovirus promoters (p10 or polh) allowing high levels of expression, while no contaminating baculovirus virions (BV/ODV) are produced.

EXAMPLES

Example I

Materials and Methods

Insect Cells and Viruses

[0099] Spodoptera frugiperda (Sf9) cells were maintained in SF900-II serum-free medium (Invitrogen) under standard conditions. Recombinant bacmid-derived AcMNPV virus (AcMNPV-EGFP) carrying an egfp reporter gene under control of the very late polyhedrin promoter transposed into the polyhedrin locus was obtained from Pijlman et al. (2006). The virus was propagated and its titers were determined by an end-point dilution assay in Sf9 cells.

In Vitro Synthesis of dsRNA

[0100] The method used to synthesize dsRNA is similar to that described by Ramadan et al. (2007) with minor modifications. All DNA templates were PCR amplified using primers with twenty-five nucleotide overhangs homologous to the T7 RNA polymerase promoter sequence 5'-gcttctaatacgactcactataggg-3'. The sequences of the primers indicated below are given in Table 1. The following primers were used for amplifying these genes: primers vp39-F and vp39-R for vp39; primers 45510 and 46235 for vp1054, primers 90292 and 90889 for vp80; primers ec-27-F and ec-27-R for odv-ec27; and primers dbp-F and dbp- for dbp. To test the efficiency of the RNAi studies we made dsRNA against egfp with primers gfp-F and gfp-R, and to have a negative control we made dsRNA with primers cat-F and cat-R for the chloramphenicol acetyl transferase (cat) gene.

[0101] The PCR products were purified using the Illustra GFX PCR DNA and Gel Band Purification Kit (GE Healthcare, Buckinghamshire, UK) and were used as templates for dsRNA in vitro synthesis using the T7 RiboMAX.TM. Express RNAi System (Promega, Madison, Wis., USA) according to manufacturer's protocol. Briefly, approximately 1 .mu.g of purified DNA templates were used for RNA synthesis at 37.degree. C. for 4 h. After synthesis, DNA templates were removed by digestion with DNase. Complementary RNA strands were annealed by incubation at 70.degree. C. for 10 min followed by slow cooling to room temperature (.about.30 min). Non-annealed (single-stranded) RNA molecules were degraded by RNase A treatment (30 min, 37.degree. C.). Finally, the dsRNA was isopropanol precipitated, resuspended in DEPC-treated sterile water to a final concentration of 0.5-1 mg/ml, and its purity and integrity were checked by agarose gel electrophoresis. The dsRNA was kept at -80.degree. C. in aliquots of 40 .mu.l. Immediately before transfection, the dsRNA was thawed on ice.

RNAi Procedure in Baculovirus-Infected Insect Cells

[0102] Sf9 cells were seeded in 24-well tissue culture plates (2.times.10.sup.5 cells/well) in 1 ml Sf900-II culture medium without serum at 28.degree. C. After two hours, the culture medium was removed, and the cells were infected with recombinant baculovirus AcMNPV-EGFP at a multiplicity of infection (MOI) of 10 TCID.sub.50 units/cell for 1 h, under standard conditions. One hour post infection (p.i.), dsRNA (20 .mu.g/well) was introduced into the cells by Cellfectin.TM.-based (Invitrogen) transfection in Grace's serum-free medium. After 4 h, the transfection mixture was replaced with Sf900-II serum-free medium. The cells were incubated for a total of 48 h p.i. at 28.degree. C. and then harvested by centrifuging at 1000.times.g for 5 min for Western blot and electron microscopy analysis. However, one fifth of the culture medium was harvested at 36 h p.i., and used for titration of budded virions by end-point dilution assays or for PCR-based detection of viral DNA. In all the experiments, dsRNA corresponding to the cat gene was taken as negative control. On the other hand, egfp gene-specific dsRNA was used as positive control for the RNAi procedure.

SDS-Polyacrylamide Electrophoresis and Western Blotting

[0103] For immuno-detection, the Sf9 cells were disrupted in 125 mM Tris-HCl, 2% sodium dodecyl sulfate (SDS), 5% 2-mercapthoethanol, 10% glycerol, 0.001% bromophenol blue, pH 6.8 at 95.degree. C. for 10 min. Proteins were separated in 10% SDS-polyacrylamide gels, and subsequently transferred to Immobilon-P membranes (Millipore) by semi-dry electroblotting. Membranes were blocked for 30 min in 1.times.PBS containing 2% fat-extracted milk powder, followed by incubation for 1 h at room temperature with either rabbit polyclonal anti-GFP antiserum (Molecular Probes), rabbit polyclonal anti-VP39 antiserum, or monoclonal anti-.alpha.-tubulin antibody (Sigma-Aldrich), all diluted 1/2000 in 1.times.PBS containing 0.2% milk power. After washing (3.times.10 min) in 1.times.PBS, the membranes were incubated with 1/4000 dilution of either goat anti-rabbit IgG or rabbit anti-mouse IgG antibodies conjugated with alkaline phosphatase (Sigma). After final washing (3.times.10 min) in AP buffer (100 mM Tris-Cl [pH 9.5], 100 mM NaCl, 5 mM MgCl.sub.2), the blots were developed with 5-bromo-4-chloro-3-indolyl phosphate nitroblue tetrazolium (NBT)/5-bromo-4-chloro-3-indolylphosphate (BCIP) (Bio-Rad) according to the manufacturer's instructions.

Preparation of Viral Genomic DNA and its PCR-Based Detection

[0104] Two-hundred microliters of cell culture medium were collected at 36 h p.i. and used for preparation of viral DNA. The cells and cell debris were removed from samples by centrifuging at 1000.times.g for 5 min. Supernatants containing budded virions were quantitatively transferred to new sterile tubes and centrifuged again at 12000.times.g for 90 min. Pelleted BVs were re-suspended in 200 .mu.l TE buffer (10 mM Tris-HCl [pH 7.5], 1 mM EDTA) containing Proteinase K (540 .mu.g/ml), and incubated at 55.degree. C. for 2 h. A phenol:chloroform:isoamyl alcohol (25:24:1) and a chloroform extraction were subsequently performed. The DNA was precipitated by adding an equal amount of isopropanol and the pellet was washed with 70% ethanol. The DNA pellet was dissolved in 15 .mu.l sterile water, and 2 .mu.l of the final DNA solution was applied to PCR-based detection of the vp39 gene sequence using primers mentioned above. All PCR reactions were performed in 25 .mu.l volumes including: 2 .mu.l DNA, 200 .mu.M dNTPs, 10 pmol of each primer, 1.5 mM MgCl.sub.2 and 1.5 U GoTaq DNA polymerase (Promega). Amplification conditions were as follows: an initial denaturation at 94.degree. C. for 2 min, after which 30 cycles of denaturation (30 s at 94.degree. C.), primer annealing (20 s at 60.degree. C.) and primer extension (25 s at 72.degree. C.). The termination cycle was 7 min at 72.degree. C. Negative controls were included in all PCR amplifications to test for contaminants in the reagents. Aliquots (3.0 .mu.l) of the PCR products were analysed by electrophoresis in 1.2% (w:v) agarose gels, with 1.times.TAE buffer, stained with ethidium bromide (0.5 .mu.g/ml).

Generation of an Antibiotic Resistance Gene-Free AcMNPV Vp80-Null Bacmid

[0105] To determine whether the VP80 protein has an essential role in the context of viral progeny production, we constructed an AcMNPV bacmid (derived from bMON14272 (from Invitrogene)) with a deletion of the vp80 ORF by homologous recombination in E. coli. To accomplish this, a cat gene flanked by mutant LoxP sites (Suzuki et al., 2005) was amplified using PCR primers vp80-KO-F and vp80-KO-R (see Table 1) from a plasmid comprising a cat gene flanked by mutant LoxP sites. The resulting PCR fragment, which contained the cat gene flanked by mutant LoxP sites and AcMNPV .about.50-bp homology sequences to the 5' or 3' proximal region of the vp80 ORF, was treated with DpnI and gel-purified to eliminate the template plasmid. The PCR product was then transformed into DH10 E. coli cells containing bMON14272 (Invitrogen) and the Lambda RED recombinase-producing plasmid pKD46 (Datsenko & Wanner, 2000), which had been prepared in the following manner. Transformed DH10 -bMON14272/pKD46 E. coli cells were grown in 50-ml LB (2.0% peptone, 0.5% yeast extract, 85.5 mM NaCl, [pH 7.0]) cultures with kanamycin (50 .mu.g/ml), ampicillin (100 .mu.g/ml) and L-arabinose (1.5 mg/ml) at 30.degree. C. to an OD.sub.600 of .apprxeq.0.6 and then made electrocompetent by a standard procedure. The electroporated cells were incubated at 37.degree. C. for 3 h in 3 ml LB medium and plated on LB-agar containing chloramphenicol at a concentration of 6.5 .mu.g/ml. After 48-h incubation at 37.degree. C., the chloramphenicol-resistant colonies were streaked to fresh LB-agar medium with 34 .mu.g/ml chloramphenicol. The plates were incubated at 37.degree. C. overnight, and colonies resistant to chloramphenicol were selected for further confirmation of the relevant genotype by PCR. Primers 90292 and 90889 were used to confirm the absence of the vp80 ORF, and primers cat-F and cat-R were employed to verify the presence of cat cassette into bacmid (detailed sequences in Table 1).

[0106] To eliminate the introduced antibiotic resistance gene (cat) from the bacmid backbone, a Cre/LoxP recombinase system was employed. A Cre recombinase-carrying plasmid pCRE obtained from Jeanine Louwerse (LUMC 0, The Netherlands) was introduced into DH10b-bMON14272-vp80null E. coli cells, and CRE expression was subsequently induced by the addition of isopropyl thiogalactoside (IPTG). Briefly, the electroporated cells were incubated at 37.degree. C. for 3 h in 3 ml of LB medium (2.0% peptone, 0.5% yeast extract, 85.5 mM NaCl, [pH 7.0]) and plated on LB-agar medium containing 50 .mu.g/ml kanamycin, 100 .mu.g/ml ampicillin and 2 mM IPTG. After 24-h incubation, colonies resistant to kanamycin and ampicillin were selected for further verification of the desired genotype by PCR. In PCR-based analysis, primers 89507 and 91713 (Table 1) were used to verify elimination of cat gene from bacmid backbone. Positive clones were also confirmed by DNA-sequencing.

[0107] To recover transposition competence, the helper transposase-encoding plasmid pMON7124 (Invitrogen) was re-introduced into DH10 -bMON14272-vp80null E. coli cells. Finally, the egfp reporter gene was introduced into the vp80-null bacmid to facilitate observation of its behaviour in insect cells. Briefly, the egfp reporter gene was amplified using PCR oligonucleotides gfp-NheI-F and gfp-SphI-R (Table 1) from plasmid pEGFP-N3 (Clontech). The PCR product was cloned into plasmid pJet1.2/Blunt using CloneJET.TM. PCR Cloning Kit (Fermentas) according to manufacturer's protocol. Subsequently, the egfp ORF was excised from error-free pJet1.2-egfp with NheI and SphI and subcloned into NheI/SphI-digested pFastBacDUAL (Invitrogen), to generate plasmid pFB-egfp. An expression cassette containing the egfp reporter gene under transcriptional control of the very late p10 promoter was transposed from pFB-egfp into polyhedrin locus of vp80-null bacmid as described in the Bac-to-Bac manual (Invitrogen). In the resulting genome, the complete vp80 ORF has been removed (see FIG. 2). This corresponds to the deletion of 2074 bp from nucleotide positions 89564 to 91637 in the AcMNPV clone C6 genome provided in SEQ ID NO: 1.

Construction of Repaired Vp80-Null Bacmids

[0108] To prepare vp80 repair donor vectors, we modified plasmid pFB-egfp (noted above) by removing the polyhedrin promoter and replacing it with a fragment containing the vp80 promoter region and the vp80 ORF. First, a 2300-bp fragment containing both the vp80 promoter and ORF sequence was amplified using primers pvp80-StuI-F and vp80-XbaI-R (Table 1) from bacmid bMON14272 template, and cloned into vector pJet1.2/Blunt (Fermentas) to form pJet1.2-pvp80-vp80. After DNA sequence verification, the vp80 cassette was excised from pJet1.2-pvp80-vp80 by StuI/XbaI double digestion, and then subcloned into Bst1107I/XbaI-digested and gel-purified pFB-egfp to generate donor plasmid pFB-egfp-pvp80-vp80. Parallelly, a donor plasmid pFB-egfp-polh-vp80, where vp80 ORF is driven by the very late polyhedrin promoter (polh) was constructed. To this aim, a 2105-bp fragment carrying the vp80 ORF was amplified using primers vp80-SacI-F and vp80-XbaI-R (Table 1) and cloned into pJet1.2/Blunt, to generate pJet1.2-vp80. In the final step, the vp80 ORF was cut out (SacI/XbaI) from pJet1.2-vp80, and subcloned into SacI/XbaI-digested pFB-egfp, to create pFB-egfp-poIH-vp80.

[0109] To overcome a problem associated with the unavailability of anti-VP80 antibody, FLAG tag decoration (N- and C-terminus fusion) of VP80 was performed to facilitate immunodetection. The N-terminally fused FLAG-vp80 sequence was generated by a double-step PCR strategy, a so-called fusion PCR. First, a 259-bp fragment containing the vp80 promoter and the FLAG tag was PCR amplified using primers pvp80-StuI-F and vp80-FLAG-R1 from the bMON14272 bacmid template. After gel-purification and DNA quantification, the 259-bp fragment was used as forward primer in a second step PCR amplification with the reverse primer vp80-XbaI-R on the bMON14272 bacmid template. The final PCR product (2324 bp) was cloned into vector pJet1.2/Blunt (Fermentas) to form pJet1.2-pvp80-FLAG-vp80. After DNA sequence verification, the FLAG-vp80 cassette was excised from pJet1.2-pvp80-FLAG-vp80 by StuI/XbaI double digestion, and then subcloned into Bst1107I/XbaI-digested and gel-purified pFB-egfp to generate donor plasmid pFB-egfp-pvp80-FLAG-vp80. The C-terminally fused vp80-FLAG cassette was amplified using pvp80-StuI-F and vp80-FLAG-R from the bMON14272 bacmid template. The 2324-bp fragment was cloned into pJet1.2/Blunt, and subsequently transferred into pFB-egfp in a similar way as previous constructs.

[0110] The inserts of all developed donor plasmids were transposed into the vp80-null bacmid following the Bac-to-Bac protocol (Invitrogen). Screening of transposition-positive constructs into the polh locus was done by a triplex PCR-based assay employing a M13 forward and reverse primers and a gentamicin resistance gene-specific primer GenR (Table 1).

Transfection-Infection Assay

[0111] Bacmid DNAs were prepared from 1.5-ml over-night bacterial cultures of 2 to 3 independent colonies carrying the bacmid with the inserted heterologous gene according to the Bac-to-Bac manual (Invitrogen) and were analyzed in parallel. For transfections, 1 .mu.g of each bacmid DNA preparation was used to transfect 1.times.10.sup.6 Sf9 cells in a 6-well plate by the Cellfectin.TM.-based transfection protocol as described in the Bac-to-Bac (Invitrogen) manual. From 72 h to 120 h post transfection (p.t.), viral propagation was checked by fluorescence microscopy. At 120 h p.t., the cell culture medium was centrifuged for 5 min at 2000.times.g to remove cell debris, and this clarified supernatant was used to infect 1.5.times.10.sup.6 Sf9 cells in 6-well plates. After 72 h p.i., the spread of virus infection was again monitored by fluorescence microscopy. In all experiments, a wild-type bMON14272 bacmid carrying the egfp reporter gene under control of the p10 promoter was used as positive control. A bMON14272-gp64null bacmid also carrying the egfp reporter gene under control of the p10 promoter served as negative control, since it has lost the ability of cell-to-cell movement of the infection (Lung et al., 2002).

Time-Course Characterization of Viral Propagation in Cell Culture

[0112] Time course analyses were performed to compare budded virus production of the AcMNPV-vp80null virus and the various repair constructs in comparison to the wild type AcMNPV bacmid (Ac-wt) all containing egfp. Briefly, the Sf9 cells were seeded in 6-well tissue culture plates (1.times.10.sup.6 cells/well in 1 ml Sf900-II culture medium without serum at 28.degree. C.). After two hours, the culture medium was removed, and the cells were transfected with 5 .mu.g bacmid DNA, under standard conditions as recommended in the Bac-to-Bac manual (Invitrogen). Cell culture supernatants were harvested at 24, 48, 72, 96 and 120 h p.t., and analysed for the production of infectious budded virus by an end-point dilution assay to determine the tissue culture infective dose 50 (TCID.sub.50). Infection was determined by monitoring egfp expression (from the p10 promoter). The average values of infectious titers derived from three independent transfections were calculated and plotted into graphs.

Transmission Electron Microscopy

[0113] Insect Sf9 cells were seeded in 25T flask (3.5.times.10.sup.6 cells/flask), and transfected with 20 .mu.g either the Ac-.DELTA.vp80, rescue Ac-.DELTA.vp80-vp80 or Ac-wt bacmid construct. After 48 h p.t., the cells were harvested and prepared for transmission electron microscopy as described previously (van Lent et al., 1990). Samples were examined and photographed with a Philips CM12 electron microscope.

Budded Virus Production Assay

[0114] Insect Sf9 cells were seeded in two 25T flasks (3.5.times.10.sup.6 cells/flask), and transfected with 20 .mu.g either Ac-.DELTA.vp80, Ac-.DELTA.vp80-vp80, Ac-.DELTA.vp80-pH-vp80, Ac-.DELTA.vp80-FLAG-vp80, Ac-.DELTA.vp80-vp80-FLAG, or Ac-wt bacmid construct. Five days p.t., the BV-enriched cell culture supernatants were harvested, and ultracentrifuged through a cushion of 10% sucrose solution (25,000 rpm for 1.5 hour, Beckman SW32). Pelleted budded virions were resuspended in sterile demi-water, and prepared for either negative staining electron microscopy, SDS-polyacrylamide electrophoresis, or PCR-based detection (as mentioned above).

Purification of ODVs and Rod-Shaped Structures from Infected Cells

[0115] The presence of ODVs and rod-like structures in infected/transfected insect cells was analyzed by electron microscopy (EM). For this purpose, insect cells were harvested 48 h p.i., lysed and the cell lysates were ultracentrifuged through a 40% sucrose cushion in TE (1 mM Tris-HCl pH 7.4, 0.1 mM EDTA) buffer (45,000 rpm for 1 hour, Beckman SW55). Pellets were resuspended in sterile demi-water and analyzed by negative staining EM as described previously (van Lent et al., 1990).

Development of Transgenic Sf9-Derived Cell Line Expressing Vp80

[0116] To develop a cell line, which produces the VP80 protein, a 2105-bp fragment carrying the vp80 ORF was amplified using primers vp80-SacI-F and vp80-XbaI-R (Table 1) and cloned into pJet1.2/Blunt, to generate pJet1.2-vp80. In the next step, the vp80 ORF was cut out (SacI/XbaI) from pJet1.2-vp80, and subcloned into SacI/XbaI-digested pIZ (Invitrogen), to create pIZ-vp80. The resulting plasmid vector pIZ-vp80 was linearized with Eco57I, and gel-purified. Sf9 cells were seeded in a six-well plate (1.times.10.sup.6 cells/well), and transfected with 10 .mu.g of the linearized vector. After 24 hours post-transfection, cells were selected by cell culture medium containing Zeocin.TM. (300 .mu.g/ml) for 2 to 3 weeks, until no control Sf9 cells survived under the same conditions. Cells were then propagated as an uncloned cell line.

Generation and Characterization of a AcMNPV Vp39-Null Bacmid

[0117] To study the role of the vp39 gene in the context of viral progeny production and the nucleocapsid assembly process, we constructed an AcMNPV bacmid (bMON14272) with a deletion of vp39 by homologous recombination in E. coli according to the same procedure as noted above for the AcMNPV vp80null bacmid construct. Since the sequence of the vp39 ORF is overlapping with promoter sequences of both flanking ORFs (cg-30 and lef-4), only an internal part of the vp39 ORF could be deleted, to avoid de-regulations of cg-30 and lef-4 expression. To reach this, a cat gene flanked by mutant LoxP sites was amplified using PCR primers vp39-KO- and vp39-KO-R (Table 1) from a plasmid comprising a cat gene flanked by mutant LoxP sites. The resulting PCR fragment, which contained the cat gene flanked by mutant LoxP sites and .about.50-bp sequences homologous to an internal region of the vp39 ORF, was treated with DpnI and gel-purified to eliminate the template plasmid. The PCR product was then transformed into DH10 E. coli cells containing bacmid bMON14272 (Invitrogen) and Lambda RED recombinase-producing plasmid pKD46 (Datsenko & Wanner, 2000) prepared in the above mentioned manner. In the final step, colonies resistant to kanamycin were subjected to PCR-based analysis using primers 75834 and 76420 (Table I) to verify insertion/elimination of the cat gene from the bacmid backbone. Positive clones were further verified by DNA-sequencing of the obtained PCR products. According to this protocol, an internal part (498 nt=166 aa) of the vp39 ORF was removed, coordinates: 75894-76391 as indicated in FIG. 9.

Construction and Analysis of Repaired Vp39-Null Bacmids

[0118] To prepare a vp39 repair donor vector, we modified plasmid pFB-egfp (noted above) by introduction of the vp39 ORF under control of the polyhedrin promoter. Initially, a 1073-bp fragment was amplified using primers vp39-SacI-F and vp39-XbaI-R (see Table I for primer sequences) from the bMON14272 template, and cloned into vector pJet1.2/Blunt (Fermentas) to form pJet1.2-vp39. After DNA sequence verification, the vp39 ORF was excised from pJet1.2-vp39 by SacI/XbaI double digestion, and then subcloned into SacI/XbaI-digested and gel-purified pFB-egfp to generate donor plasmid pFB-egfp-vp39. After an unsuccessful attempt to rescue AcMNPV vp39null with pFB-egfp-vp39, a set of novel donor plasmids was prepared. First, a 2498-bp fragment containing vp39 and lef-4 ORFs was PCR-generated using primers vp39-StuI-F and lef-4-XbaI-R from bacmid bMON14272 template, and cloned into vector pJet1.2/Blunt (Fermentas) to form pJet1.2-vp39-lef-4. After DNA sequence confirmation, the fragment containing vp39 and lef-4 ORFs was excised from pJet1.2-vp39-lef-4 by StuI/XbaI double digestion, and then subcloned into StuI/XbaI-digested and gel-purified pFB-egfp to generate donor plasmid pFB-egfp-vp39-lef-4.

[0119] Parallelly, donor plasmid pFB-egfp-vp39-cg30 was constructed, where both vp39 and cg-30 ORFs are driven from the very late polyhedrin promoter, and the cg-30 ORF can also use its native promoter situated inside the 3'-end of the vp39 ORF. Briefly, a 1868-bp fragment carrying both vp39 and cg-30 ORFs was amplified using primers cg30-XbaI-F and vp39-XbaI-R (noted above) and cloned into pJet1.2/Blunt, to generate pJet1.2-vp39-cg30. The vp39/cg-30 cassette was subcloned as SacI/Xba into pFB-egfp, to create pFB-egfp-vp39-cg30. Additionally, a similar donor vector pFB-egfp-FLAG-vp39-cg30 was constructed, where vp39 ORF is N-terminally FLAG-tagged. The same strategy was employed to develop this vector, only the reverse primer vp39-FLAG-SacI-R was used to amplify vp39/cg-30 cassette instead of the vp39-XbaI-R primer.

[0120] All developed donor plasmids were transposed into vp39-null bacmid following the Bac-to-Bac kit protocol (Invitrogen) and screened as detailed above for vp80 repair bacmids. The functional analysis was performed as described above for the vp80 constructs.

Generation and Analysis of AcMNPV Vp1054-Null Bacmid

[0121] To verify the essential role of the vp1054 gene in the context of viral progeny production and nucleocapsid assembly, we constructed an AcMNPV bacmid (bMON14272) with a deletion of vp1054 by homologous recombination in E. coli according to the same procedure as for the vp80null bacmid construct with minor alternations. Since the vp1054 ORF is overlapping with the essential lef-10 ORF, we could not remove the whole vp1054 ORF, but only a 955-bp nucleotide 3'-end part of the ORF. To prevent translation of the C-truncated VP1054 mutant in insect cells, we decided to mutate the first translation codon ATG.fwdarw.Met to ACG.fwdarw.Thr. This single nucleotide substitution also changed an internal codon no. 32 (AAT) to AAC of lef-10 ORF, however, both are encoding the same amino acid (Asn). To accomplish this, we first amplified the 5'-end of the vp1054 ORF using primers vp1054-KO-F and vp1054-KO-R1 from bacmid bMON14272 (Invitrogen). The 214-bp PCR product contained a mutation of the ATG start codon of the vp1054 ORF, introduced a synthetic stop/poly-A signal sequence for the lef-10 ORF, and has a 3'-end sequence homology overhang to the cat cassette to facilitate the second PCR, and a 49-bp homology sequence to the 5'-end of vp1054 ORF to mediate Lambda RED-directed homologous recombination in E. coli. After gel-purification and DNA quantification, the 214-bp fragment was used as forward primer in a second step PCR with reverse primer vp1054-KO-R2 with a plasmid comprising a cat gene flanked with mutant LoxP sites as template. The resulting 1230-bp PCR fragment, which contained the cat gene flanked by mutant LoxP sites, a mutated 5'-end of the vp1054 ORF and .about.50-bp sequences homologous to the 5' or 3' proximal region of the vp1054 ORF, was treated with DpnI and gel-purified to eliminate the template plasmid. Recombination of this PCR product with the bMON14272 bacmid was performed as described above for the vp80 mutant. Kanamycin resistant colonies were verified by PCR with primer pairs cat-F/cat-R, 45510/46235, and 45122 and 46441 to check the insertion/elimination of the cat gene from the bacmid backbone. Insertion sites were also confirmed by DNA-sequencing. This method resulted in the deletion of 955 bp from nucleotide positions 45365 to 46319 in the AcMNPV clone C6 genome provided in SEQ ID NO: 1. All primer sequences are given in Table 1.

Construction of a Repaired Vp1054-Null Bacmid Construct

[0122] To prepare vp1054 repair donor vector, we modified plasmid pFB-egfp (noted above) by removing the polyhedrin promoter and replacing it with a fragment containing the vp1054 promoter region and the vp1054 ORF. First, a 1714-bp fragment containing both the vp1054 promoter and ORF sequence was amplified using primers vp1054-Rep-F and vp1054-Rep-R from bacmid bMON14272 template, and cloned into vector pJet1.2/Blunt (Fermentas) to form pJet1.2-pvp1054-vp1054. After DNA sequence verification, the vp1054 cassette was excised from pJet1.2-pvp1054-vp1054 by StuI/XbaI double digestion, and then subcloned into Bst1107I/XbaI-digested and gel-purified pFB-egfp to generate donor plasmid pFB-egfp-pvp1054-vp1054. The developed donor plasmids were transposed into the vp1054-null bacmid following the Bac-to-Bac protocol (Invitrogen) and screened. Recombinant bacmids were analyzed as detailed above for vp80 bacmids.

Generation and Analysis of AcMNPV p6.9-Null Bacmid

[0123] To verify the essential role of p6.9 in the context of viral progeny production, we constructed an AcMNPV bacmid (bMON14272) with a deletion of p6.9 by homologous recombination in E. coli. To accomplish this, a chloramphenicol resistance gene (cat) flanked by mutant LoxP sites was amplified using PCR primers p6.9-KO-F and p6.9-KO-R from a plasmid comprising a cat gene flanked by mutant LoxP sites. Mutant viruses were obtained following the same procedure as for the other mutants. For the PCR-based analysis of the finally obtained mutant clones the primer pairs cat-F and cat-R and 86596 and 86995 were used to check insertion/elimination of cat gene from bacmid backbone. Positive clones were also confirmed by DNA-sequencing. This method results in the deletion of 164 bp from nucleotide positions 86716 to 86879 in the AcMNPV clone C6 genome provided in SEQ ID NO: 1. Table 1 for primer sequences.

Construction and Functional Analysis of Repaired p6.9-Null Bacmids

[0124] To prepare p6.9 repair donor vectors, the pFB-GFP-p6.9 vector was used, which was constructed by Marcel Westenberg (Wageningen University). To make this vector, the AcMNPV p6.9 promoter sequence was amplified from the plasmid pAcMP1 (Hill-Perkins & Possee, 1990) with primers pp6.9-F and pp6.9-R using the high-fidelity Expand long-template PCR system (Roche). The PCR product was cloned as SalI fragment into pFastBac1 (Invitrogen), from which the polyhedrin promoter was deleted in advance by fusing the Bst1107I to the StuI site, to obtain pFB1-p6.9. The p6.9 promoter from pFB1-p6.9 was recloned as SnaBI/BamHI fragment into the Bst1107I and BamHI sites of pFastBacDUAL (Invitrogen), thereby deleting the polyhedrin promoter. Subsequently, the egfp reporter gene was cloned downstream of the p10 promoter into the XmaI site to obtain pFB-GFP-p6.9. Finally, the p6.9 genes of AcMNPV and Spodoptera exigua (Se)MNPV were PCR amplified from either the AcMNPV bacmid (bMON14272) or SeMNPV genomic DNA by using the high-fidelity Expand long-template PCR system and primers generating EcoRI and NotI at the 5' and 3' ends, respectively (Table 1). The PCR products were cloned downstream of the p6.9 promoter in the EcoRI/NotI sites of pFB-GFP-p6.9. All generated clones were sequenced to verify the incorporated p6.9 sequences.

[0125] The expression cassettes of both developed donor plasmids were transposed into the p6.9-null bacmid following the Bac-to-Bac protocol (Invitrogen). Screening of transposition-positive constructs into the polh locus was done by the triplex PCR-based assay as described above for the vp80 constructs. The analysis was performed as for the vp80 constructs

Results

[0126] Silencing of AcMNPV Vp80 does not Affect Baculovirus Very Late Gene Expression

[0127] We explored the effect of transfecting Sf9 cells with different dsRNAs during infection with AcMNPV-GFP. To trigger dsRNA-induced silencing of selected baculoviral genes (vp1054, vp39, vp80, dbp and odv-ec27), we generated gene-specific dsRNAs using in vitro T7 RNA polymerase-based synthesis. However, when we began these studies it was not clear what amount and time point of dsRNA transfection is the most effective to silence baculoviral genes. To determine an optimal amount of dsRNA for RNAi assay purposes in baculovirus-infected cells, we first attempted to silence reporter egfp gene with different amounts of dsRNA. These pilot assays showed that the most potent RNAi effect is achieved using 100 pg dsRNA per cell (data not shown). At the same time, it was also proved that RNAi treatment has no negative effect on the production of infectious budded virions progeny. We also tried to transfect dsRNA into the cells at two different time points, 24 h prior to infection or 1 h p.i. The results proved that transfection performed at 1 h p.i. is more efficient in silencing of genes expressed at late/very late phases of baculoviral infection in contrast to transfection carried out at 24 h prior to infection (data not shown). In addition, to ensure that knock-down was gene-specific, dsRNA corresponding to the cat gene was transfected as an RNAi negative control. Herein, we could observe a moderate inhibition of baculovirus infection propagation in comparison to untransfected insect cells. However, the same phenomenon was also observed when insect cells were treated only with transfection reagents. Therefore, we could conclude that the effect can be explained by a negative impact (cytotoxicity) of the presence of transfection reagents on cell viability.

[0128] Silencing screening of baculovirus genes revealed that down-regulation of vp1054, vp39, dbp and odv/ec-27 is also associated with a reduction or inhibition of very late gene expression measured by EGFP detection (FIGS. 1A and 1B). The highest levels of this inhibition were observed in dbp- and odv/ec-27-targeted cells. The cause of this effect can be explained by the presence of bi-cistronic and overlapping mRNA transcripts, which are produced during a baculovirus replication cycle. Eventually, a cross-reaction with targets of limited sequence similarities can also be involved in the process. Only cells treated with vp80 dsRNA showed a similar level of EGFP expression as untransfected cells or particularly with cat dsRNA-treated cells. Importantly, very few EGFP-producing cells were observed in insect cells where egfp-specific dsRNA was introduced (positive RNAi control), showing that the transfection efficiency was high. Based on our RNAi screening achievements, the vp80 gene (locus) seems to be a suitable candidate for RNAi-based targeting in context of interference with baculoviral very late gene expression.

Knock-Down of Vp80 Totally Prevents Production of BVs and Normally Appearing ODVs

[0129] To determine the roles of selected candidate genes (vp1054, vp39, vp80, dbp and odv/ec-27) in production of budded virions progeny, cell culture medium (36 h p.i.) from dsRNA-treated cells was examined for the presence of BVs. End-point dilution-based titrations confirmed that all tested genes are essential for infectious budded virus progeny production (FIG. 1C). We were not able to detect any infectious BVs in vp80- and dbp-targeted cells. In addition, PCR-based assay indicated that defective or non-infectious viral particles are also not produced in vp80-targeted cells. It is important to point out that the results also showed a significant decrease in the production of infectious BVs in the RNAi controls (egfp- and cat-specific dsRNA-treated cells) compared to untransfected cells. The cytotoxicity of transfection reagents is again the assumed cause of this negative effect. Electron microscopy analysis of cell lysates showed that formation of ODVs and rod-like structures was totally inhibited in cells treated with dsRNA-vp39 as expected (FIG. 1D). Production of ODVs and rod-like structures was also significantly reduced in insect cells treated with dsRNA-vp80 (FIG. 1D). However, in vp80-targeted cells we could mostly find nucleocapsids of aberrant phenotypes (pointed shape). On the other hand, introduction of dsRNA-cat into insect cells did not cause any changes in the production of ODVs.

The AcMNPV Vp80 Gene is Essential for Viral Replication

[0130] An AcMNPV deletion virus was constructed as detailed in FIG. 2. Repair constructs were designed such that the wild-type vp80 ORF or N- and C-terminally FLAG-tagged vp80 genes along with its native or polyhedrin promoter regions were inserted into the polyhedrin locus along with the egfp gene under the p10 promoter (FIG. 3A). To investigate the function of the vp80 gene, Sf9 cells were transfected with either the knock-out or repair bacmid constructs and monitored for EGFP expression by fluorescence microscopy. When Ac-vp80 null was introduced into Sf9 cells, no viral propagation was observed in cell culture at 72 h to 120 h p.t. We could observe only a "single-cell infection" phenotype similar to the phenotype of Ac-gp64null bacmid (FIG. 3B). The results indicate that Ac-vp80null is able to reach the very late phase of infection as confirmed by p10 promoter-driven EGFP expression. From 72 h to 120 hours p.t., widespread EGFP expression could be seen in insect cell monolayers that were transfected with the three repair (vp80 driven from its native promoter, vp80 driven from polyhedrin promoter and N-terminally FLAG-tagged vp80 driven from its native promoter) constructs indicating that these bacmids were able to produce levels of infectious budded virions sufficient to initiate secondary infection at a similar level as the wild-type bacmid (FIG. 3B). In contrast, in insect cells transfected with C-terminally FLAG-tagged vp80 repair constructs, by 72 h p.t. EGFP expression was only observed in isolated cells that were initially transfected indicating that this bacmid construct is defective in viral replication (FIG. 3B). However, by 96 h p.t. formation of tiny plaques was observed and by 120 h p.t. very few plaques of normal size were developed. The results show that the C-terminally flagged mutant is strongly delayed in producing budded virus and showed that an unmodified C-terminus is very important for the function of VP80. At 5 days p.t., cell culture supernatants were removed and added to freshly plated Sf9 cells and then incubated for 3 days to detect infection by virus generated from cells transfected with these bacmids. As expected, Sf9 cells incubated with supernatants from the transfections with repair constructs showed numerous EGFP expressing cells (FIG. 3C). Nevertheless, cells incubated with supernatant from C-terminally FLAG-tagged constructs showed a significant reduction in the number of EGFP-positive cells. On the other hand, in insect cells incubated with supernatant from the transfection with the vp80 knockout, no EGFP expression was detected at any time-point analyzed up to 72 h (FIG. 3C).

[0131] Moreover, to characterize the exact effect of deletion of the vp80 gene on AcMNPV infection, the viral propagation in transfected Sf9 cells was compared between Ac-wt, Ac-.DELTA.vp80, Ac-.DELTA.vp80-vp80Rep, Ac-.DELTA.vp80-polh-vp80Rep, Ac-.DELTA.vp80-FLAG-vp80Rep and Ac-.DELTA.vp80-vp80-FLAGRep. Cell culture supernatants of all the above bacmid constructs were analysed at indicated time points for BV production (FIG. 4). As expected, the repaired Ac-.DELTA.vp80-vp80Rep, Ac-.DELTA.vp80-polh-vp80Rep, Ac-.DELTA.vp80-FLAG-vp80Rep viruses showed kinetics of viral replication consistent with wild-type virus (Ac-wt) propagation. Budded virion production by the C-terminally flagged Ac-.DELTA.vp80-vp80-FLAGRep virus was reduced to approximately 0.06% compared to the Ac-wt virus or the other repaired viruses.

[0132] These results indicate that the vp80 gene is essential for infectious BV production. It has clearly been proven that the whole sequence of vp80 ORF can completely be deleted from the bacmid backbone and adequately rescued by introduction of the vp80 ORF into a heterologous site (polyhedrin locus) of the genome. We also showed that vp80 gene expression can be driven by the heterologous polyhedrin promoter sequence with no negative effect on viral replication in cell culture. Additionally, we observed that the N-terminus in contrast to the C-terminus of VP80 is permissive to gene modifications (epitope tag-labeling). We noted that the kinetics of the C-terminally FLAG-tagged VP80 virus was significantly delayed when compared with all other rescue or wild-type viruses, indicating the functional importance of the VP80 C-terminus.

VP80 is Required for Production of Both BV and ODV

[0133] The results described above indicated that the Ac-vp80null mutant is completely defective in production of infectious budded virus. However, there was also a possibility that the mutant can still produce non-infectious budded particles. To investigate the ability, Sf9 cells were transfected with either the knock-out, repair or wild-type bacmid constructs and 7 days p.t. cell culture mediums were ultracentrifuged to pellet budded viruses. The formed pellets were either analyzed by negative staining electron microscopy or by Western blot- and PCR-based detection to confirm the presence of the budded viruses. No intact budded virus, virus-like particles, nor its structures (such as major capsid protein VP39 and viral genome sequence) were revealed in the pellet from the cells transfected with the Ac-vp80null mutant (FIGS. 5A and 5B). On the other hand, all analyzed repair constructs produced normally-appearing budded virus as compared with budded virus-derived from the wild-type virus (FIG. 5A). Nevertheless, it was very difficult to find representative budded virions in the pellet derived from C-terminally FLAG-tagged vp80 gene repair construct-transfected cells.

[0134] To further characterize deletion of the vp80 gene on baculovirus life cycle, electron microscopy was performed with ultra-thin sections generated from bacmid-transfected cells. The Ac-vp80null-transfected cells developed the typical phenotype of baculovirus-infected cells with an enlarged nucleus, a fragmented host chromatin, an electron-dense virogenic stroma, etc. (FIG. 6A). The absence of VP80 did not prevent formation of normally-appearing nucleocapsids inside the virogenic stroma (FIG. 6C). The formed nucleocapsids were phenotypically undistinguishable from those produced by either the Ac-vp80null repair or Ac-wt bacmids. However, an abundance of assembled nucleocapsids was rather less as compared with cells transfected with the Ac-vp80null repair or Ac-wt bacmids (FIGS. 6E and 6G). In addition, no occlusion-derived virions nor bundles of nucleocapsids prior to an envelopment could be observed in the peristromal compartment of a nucleoplasm (so called the ring zone) of Ac-vp80null bacmid-transfected cells (FIGS. 6B and 6D). It seems that VP80 plays a role during maturation of nucleocapsids and/or their release/transport from the virogenic stroma. Eventually, VP80 can somehow contribute to an efficient nucleocapsid assembly which could be explained by the small number of nucleocapsids present in the virogenic stroma of Ac-vp80null transfected cells. When the vp80 gene was re-introduced back into the bacmid mutant, a lot of nucleocapsids and occlusion-derived virions could be seen in the ring zones of transfected cells (FIG. 6F). An abundance and morphology of occlusion-derived virions produced in Ac-.DELTA.vp80-vp80 repair bacmid-transfected cells were similar to those produced by wild-type bacmid (FIGS. 6F and 6H).

VP80 Function can be Complemented by the Trans-Acting Vp80 Gene

[0135] To prove that VP80 function can be complemented by the trans-acting vp80 ORF, a complementation assay was performed with a transgenic cell line, Sf9-vp80, that was stably transformed with the vp80 gene expressed under control of an early baculovirus Orgyia pseudotsugata ie-2 promoter. In the assay, both Sf9 and Sf9-vp80 cells were transfected with the Ac-vp80null bacmid mutant (FIG. 7). Virus infection spread was monitored by EGFP-specific fluorescence at 72 h and 96 h p.t. In Sf9-vp80 cells we could observe viral plaques demonstrating the virus spread. On the other hand, in Sf9 cells only "single-cell infection" phenotype could be seen as previously described above. After six days, the cell culture supernatants were harvested and used as an inoculum to infect fresh groups of Sf9 cells. After 5 days, EGFP-positive cells were monitored by fluorescence microscopy. Only "single-cell infection" phenotype was observed in Sf9 cells receiving the supernatant from Sf9-vp80 cells. As assumed, no EGFP signal was detected in Sf9 cells receiving the supernatant from Sf9 cells. These results show that the Ac-vp80null can be rescued by VP80-expressing cells (Sf9-vp80) and demonstrate that the observed complementation is due to VP80 protein expressed from the host cell line and not from acquisition of the vp80 gene from the cell line. In other words, the results match requirements asked to produce biopharmaceuticals (EGFP protein in our model assay) without contaminating baculovirus virions.

Generation and Characterization of Vp39-Null Bacmid

[0136] To study the functionality of the AcMNPV vp39 gene during virus infection, a vp39-null AcMNPV bacmid was constructed by partial deletion of the vp39 gene. The deletion construct was selected by its resistance to chloramphenicol indicating that site-specific deletion of the vp39 gene had occurred. In the resulting vp39-null AcMNPV bacmid, the internal part of vp39 gene was correctly replaced by the cat gene. Subsequently, the cat was eliminated by Cre/LoxP recombination (FIG. 8A). The vp39 sequence was removed from nucleotides 75894 to 76391 according to the AcMNPV clone C6 genome sequence (SEQ ID NO:1). The structure of the vp39 deletion constructs was confirmed by PCR using primers 75834 and 76420 (FIG. 8B). A 647-bp DNA fragment was amplified when wild-type AcMNPV bacmid was used as a template, whereas a 1113-bp DNA fragment could be amplified on AcMNPV vp39-null(+cat) template (FIG. 8B). When the final construct AcMNPV-vp80null (-cat) with eliminated cat cassette was used in PCR analysis, only a short 183-bp DNA fragment could be detected (FIG. 8B). The results were confirmed by DNA sequencing.

Functional mapping of vp39 ORF indicates a presumable functional relationship between vp39 and cg-30 ORFs

[0137] The repair constructs were designed in such a way that the wild-type vp39 ORF under control of the polyhedrin promoter sequence was inserted into the polyhedrin locus along with the egfp gene controlled by the p10 promoter (FIG. 9A). To investigate the function of the vp39 gene, Sf9 cells were transfected with either the knock-out or repair bacmid constructs and monitored for EGFP expression by fluorescence microscopy. When Ac-vp39 null was introduced into Sf9 cells, no viral propagation was observed from 72 h to 168 h p.t. We could observe only a "single-cell infection" phenotype similar to the phenotype of the Ac-gp64null bacmid (FIG. 9B).

[0138] These results indicate that the Ac-vp39null construct is able to reach the very late phase of infection as shown by the p10 promoter-driven EGFP expression. Unexpectedly, no viral propagation could be seen in insect cell monolayers that were transfected with the vp39 repair (vp39 driven from polyhedrin, Ac-.DELTA.vp39-polh-vp39Rep) constructs (FIG. 3B). For this reason, we decided to prepare three extra repair bacmids carrying both vp39 and lef-4 ORFs under control of their native promoters. When the insect cells were transfected with these repair constructs again viral replication did not occur (FIG. 9B) and a "single-cell infection" phenotype was observed from 72 h to 168 h p.t. Interestingly, in insect cell monolayers that were transfected with the repair constructs carrying both vp39 (or FLAG-tagged vp39) and cg-30 we could observe tiny clusters of EGFP-positive cells (3-5 cells) (FIG. 9B). However, we did not see a full-value viral replication as that of the wild-type vector (Ac-wt),

[0139] At 7 days p.t., cell culture supernatants were collected and added to freshly plated Sf9 cells, which were then incubated for 3 days to detect infection by virus generated from cells transfected with all bacmids mentioned here (FIG. 9C). As expected, Sf9 cells incubated with the supernatant from Ac-wt transfections showed numerous EGFP expressing cells. On the other hand, cells incubated with supernatants from Ac-.DELTA.vp39-polh-vp39Rep and Ac-.DELTA.vp39-vp39-lef-4Rep constructs did not show any EGFP-positive cells. However, in insect cells incubated with supernatants from Ac-.DELTA.vp39-vp39-cg30Rep and Ac-.DELTA.vp39-FLAG-vp39-Rep, a number of EGFP-expressing cells were detected (FIG. 9C). These results indicated that a possible functional relationship between the vp39 and cg-30 ORFs is required for baculovirus replication.

[0140] Since the vp39 ORF sequence overlaps with the promoter sequences of the two flanking ORFs (lef-4 and cg-30), we could not delete the whole vp39 ORF in our vp39null bacmid construct. It may therefore also be that C- and/or N-truncated mutant(s) of vp39 may be expressed which may interfere as a competitive inhibitor with the normal VP39 protein.

Construction and Analysis of Vp1054-Null Bacmid

[0141] To study the functionality of the AcMNPV vp1054 gene during virus infection, a vp1054-null AcMNPV bacmid was constructed by partially deleting the vp1054 gene from AcMNPV bacmid (bMON14272) by homologous recombination in E. coli. The deletion construct was selected by its resistance to chloramphenicol that indicated that site-specific deletion of the vp1054 gene had occurred. In the resulting vp1054-null AcMNPV bacmid, the 955-bp 3'-end part of the vp1054 gene was correctly replaced by the cat gene. Subsequently, the antibiotic resistance cassette (cat) was eliminated from bacmid backbone using Cre/LoxP recombination system (FIG. 10A). The deleted sequence was removed from the nucleotide coordinates 45365 to 46319 according to the AcMNPV clone C6 genome sequence (SEQ ID NO:1). The structure of all the deletion constructs was confirmed by PCR (FIG. 10B). When the vp1054 gene is present, as in the parental wild-type AcMNPV bacmid, a 775-bp PCR product can be amplified using primers 45510 and 46235, whereas a 596-bp PCR fragment amplified with cat-F and cat-R primers is produced only when the cat gene was introduced into the bacmid sequence in case of AcMNPV vp1054null (+cat) construct (FIG. 10B). Correct recombination process was also confirmed by PCR mapping of vp1054 locus using primers 45122 and 46441. A 1320-bp DNA fragment was amplified when wild-type AcMNPV bacmid was used as a template, whereas a 1353-bp DNA fragment could be amplified on AcMNPV vp1054-null(+cat) template (FIG. 10B). When final construct AcMNPV-vp1054null (-cat) with eliminated cat cassette was used in PCR analysis, only a 423-bp DNA fragment could be detected (FIG. 10B). Positive clones were successfully verified by DNA sequencing.

AcMNPV Vp1054 Gene is Essential for Viral Replication

[0142] The repair construct was designed such that the AcMNPV vp1054 ORF with its native promoter region was inserted into the polyhedrin locus along with the egfp gene under the control of the p10 promoter (FIG. 11A). Since the vp1054 promoter and ORF sequences are overlapping with lef-10 ORF, the repair construct is also capable to express LEF-10. To investigate the function of the vp1054 gene, Sf9 cells were transfected with either the vp1054 knock-out or repair bacmid construct and monitored for EGFP expression by fluorescence microscopy. When Ac-vp1054 null construct was introduced into Sf9 cells, no viral propagation was observed in cell culture at 72 h to 120 h p.t. We could observe only a "single-cell infection" phenotype similar to the phenotype of Ac-gp64null bacmid (FIG. 11B). The results indicate that Ac-vp1054null is able to reach the very late phase of infection as confirmed by p10 promoter-driven EGFP expression. In other words, the results suggest that the expression of late expression factor 10, LEF-10, was not affected in vp1054-null bacmid mutant. From 72 h to 120 hours p.t., widespread EGFP expression could be seen in insect cell monolayers that were transfected with the repair constructs (Ac-.DELTA.vp1054-vp1054). The results are indicating that the repair bacmid is able to produce levels of infectious budded virions sufficient to initiate secondary infection at a similar level as the wild-type bacmid (FIG. 11B). At 6 days p.t., cell culture supernatants were removed and added to freshly plated Sf9 cells and then incubated for 3 days to detect infection by virus generated from cells transfected with these bacmids. As expected, Sf9 cells incubated with supernatants from the transfections with the repair constructs showed numerous EGFP expressing cells (FIG. 11C). On the other hand, in insect cells incubated with supernatant from the transfection with the Ac-vp1054null knockout, no EGFP expression was detected at any time-point analyzed up to 72 h (FIG. 11C).

[0143] These results indicate that the vp1054 gene is essential for infectious BV production. It has clearly been proven that the 955-bp 3'-end sequence part of the vp1054 ORF can completely be deleted from the bacmid backbone and adequately rescued by introduction of the AcMNPV vp1054 ORF into a heterologous site (polyhedrin locus) of the genome. In addition, the results proved that deletion of the vp1054 gene does not affect very late gene expression, as demonstrated by EGFP-positive cells in cells transfected with Ac-vp1054null bacmid mutant (FIG. 11B).

Generation and Characterization of p6.9-Null Bacmid

[0144] To study the functionality of the AcMNPV p6.9 gene during virus infection, a vp80-null AcMNPV bacmid was constructed by deleting the p6.9 gene from AcMNPV bacmid (bMON14272) by homologous recombination in E. coli. The deletion construct was selected by its resistance to chloramphenicol that indicated that site-specific deletion of the p6.9 gene had occurred. In the resulting p6.9-null AcMNPV bacmid, the p6.9 gene was correctly replaced by the cat gene. Subsequently, the antibiotic resistance cassette (cat) was eliminated from bacmid backbone using Cre/LoxP recombination system (FIG. 12A). The deleted sequence was removed from the translational start codon (ATG.fwdarw.Met) to the stop codon (TAT.fwdarw.Tyr), nucleotide coordinates 86716 to 86879 according to the AcMNPV clone C6 genome sequence (SEQ ID NO:1). The stop codon of the p6.9 orf was not removed since its sequence is overlapping with the stop codon of flanked lef-5 orf. The structure of all the deletion constructs was confirmed by PCR (FIG. 12 B). When the p6.9 gene is present, as in the parental wild-type AcMNPV bacmid, a 596-bp PCR fragment could be only amplified with cat-F and cat-R primers when cat gene was introduced into bacmid sequence in case of AcMNPV p6.9null (+cat) construct (FIG. 12B). Correct recombination process was also confirmed by PCR mapping of p6.9 locus using primers 86596 and 86995. A 400-bp DNA fragment was amplified when wild-type AcMNPV bacmid was used as a template, whereas a 1220-bp DNA fragment could be amplified on AcMNPV vp80-null(+cat) template (FIG. 12B). When final construct AcMNPV-vp80null (-cat) with eliminated cat cassette was used in PCR analysis, only a short 290-bp DNA fragment could be detected (FIG. 12B). Positive clones were successfully verified by DNA sequencing.

AcMNPV p6.9 Gene is Essential for Viral Replication

[0145] The repair constructs were designed such that the wild-type AcMNPV or SeMNPV p6.9 ORFs with AcMNPV p6.9 promoter region were inserted into the polyhedrin locus along with the egfp gene under the p10 promoter (FIG. 13A). To investigate the function of the p6.9 gene, Sf9 cells were transfected with either the p6.9 knock-out or repair bacmid constructs and monitored for EGFP expression by fluorescence microscopy. When Ac-p6.9 null was introduced into Sf9 cells, no viral propagation was observed in cell culture at 72 h to 120 h p.t. We could observe only a "single-cell infection" phenotype similar to the phenotype of Ac-gp64null bacmid (FIG. 13B). The results indicate that Ac-p6.9null is able to reach the very late phase of infection as confirmed by p10 promoter-driven EGFP expression. From 72 h to 120 hours p.t., widespread EGFP expression could be seen in insect cell monolayers that were transfected with the two repair constructs (Ac-.DELTA.p6.9-Acp6.9 and Ac-.DELTA.p6.9-Sep6.9). The results are indicating that these two repair bacmids are able to produce levels of infectious budded virions sufficient to initiate secondary infection at a similar level as the wild-type bacmid (FIG. 13B). At 6 days p.t., cell culture supernatants were removed and added to freshly plated Sf9 cells and then incubated for 3 days to detect infection by virus generated from cells transfected with these bacmids. As expected, Sf9 cells incubated with supernatants from the transfections with the repair constructs showed numerous EGFP expressing cells (FIG. 13C). On the other hand, in insect cells incubated with supernatant from the transfection with the Ac-p6.9null knockout, no EGFP expression was detected at any time-point analyzed up to 72 h (FIG. 3C). Moreover, to characterize the exact effect of deletion of the p6.9 gene on AcMNPV infection, the viral propagation in transfected Sf9 cells was compared between Ac-wt, Ac-.DELTA.p6.9, Ac-.DELTA.p6.9-Acp6.9Rep, and Ac-.DELTA.p6.9-Sep6.9Rep). Cell culture supernatants of all the above bacmid constructs were analysed at indicated time points for BV production (FIG. 13D). As expected, the repaired Ac-.DELTA.p6.9-Acp6.9Rep and Ac-.DELTA.p6.9-Sep6.9Rep viruses showed kinetics of viral replication consistent with wild-type virus (Ac-wt) propagation.

[0146] These results indicate that the p6.9 gene is essential for infectious BV production. It has clearly been proven that the whole sequence of p6.9 ORF can completely be deleted from the bacmid backbone and adequately rescued by introduction of the AcMNPV vp80 ORF into a heterologous site (polyhedrin locus) of the genome. We also showed that p6.9 gene can be complemented efficiently by the SeMNPV-derived p6.9 ORF (M. Westenberg). In addition, the results proved that deletion of the p6.9 gene does not affect very late gene expression, as demonstrated by EGFP-positive cells in cells transfected with Ac-p6.9null bacmid mutant (FIG. 15B).

Example II

[0147] The inventors have amended the best mode of the present invention in the following example.

Materials and Methods

Generation of an Antibiotic Resistance Gene-Free AcMNPV Vp80-Null Bacmid

[0148] To determine whether the VP80 protein has an essential role in the context of viral progeny production, we constructed an AcMNPV bacmid (derived from bMON14272 (from Invitrogen)) with a deletion of the vp80 ORF by homologous recombination in E. coli. To accomplish this, a cat gene flanked by mutant LoxP sites (Suzuki et al., 2005) was amplified using PCR primers vp80-KO-F and vp80-KO-R (see Table 1) from a plasmid comprising a cat gene flanked by mutant LoxP sites. The resulting PCR fragment, which contained the cat gene flanked by mutant LoxP sites and AcMNPV .about.50-bp homology sequences to the 5' or 3' proximal region of the vp80 ORF, was treated with DpnI and gel-purified to eliminate the template plasmid. The PCR product was then transformed into DH101 E. coli cells containing bMON14272 (Invitrogen) and the Lambda RED recombinase-producing plasmid pKD46 (Datsenko & Wanner, 2000), which had been prepared in the following manner. Transformed DH10 -bMON14272/pKD46 E. coli cells were grown in 50-ml LB (2.0% peptone, 0.5% yeast extract, 85.5 mM NaCl, [pH 7.0]) cultures with kanamycin (50 .mu.g/ml), ampicillin (100 .mu.g/ml) and L-arabinose (1.5 mg/ml) at 30.degree. C. to an OD.sub.600 of .apprxeq.0.6 and then made electrocompetent by a standard procedure. The electroporated cells were incubated at 37.degree. C. for 3 h in 3 ml LB medium and plated on LB-agar containing chloramphenicol at a concentration of 6.5 .mu.g/ml. After 48-h incubation at 37.degree. C., the chloramphenicol-resistant colonies were streaked to fresh LB-agar medium with 34 .mu.g/ml chloramphenicol. The plates were incubated at 37.degree. C. overnight, and colonies resistant to chloramphenicol were selected for further confirmation of the relevant genotype by PCR. Primers 90292 and 90889 were used to confirm the absence of the vp80 ORF, and primers cat-F and cat-R were employed to verify the presence of cat cassette into bacmid (detailed sequences in Table 1).

[0149] To eliminate the introduced antibiotic resistance gene (cat) from the bacmid backbone, a Cre/LoxP recombinase system was employed. A Cre recombinase-carrying plasmid pCRE obtained from Jeanine Louwerse (LUMC Leiden, The Netherlands) was introduced into DH10b-bMON14272-vp80null E. coli cells, and CRE expression was subsequently induced by the addition of isopropyl thiogalactoside (IPTG). Briefly, the electroporated cells were incubated at 37.degree. C. for 3 h in 3 ml of LB medium (2.0% peptone, 0.5% yeast extract, 85.5 mM NaCl, [pH 7.0]) and plated on LB-agar medium containing 50 .mu.g/ml kanamycin, 100 .mu.g/ml ampicillin and 2 mM IPTG. After 24-h incubation, colonies resistant to kanamycin and ampicillin were selected for further verification of the desired genotype by PCR. In PCR-based analysis, primers 89507 and 91713 (Table 1) were used to verify elimination of cat gene from bacmid backbone. Positive clones were also confirmed by DNA-sequencing.

[0150] To recover transposition competence, the helper transposase-encoding plasmid pMON7124 (Invitrogen) was re-introduced into DH10 -bMON14272-vp80null E. coli cells. Finally, the egfp reporter gene was introduced into the vp80-null bacmid to facilitate observation of its behaviour in insect cells. Briefly, the egfp reporter gene was amplified using PCR oligonucleotides gfp-NheI-F and gfp-SphI-R (Table 1) from plasmid pEGFP-N3 (Clontech). The PCR product was cloned into plasmid pJet1.2/Blunt using CloneJET.TM. PCR Cloning Kit (Fermentas) according to manufacturer's protocol. Subsequently, the egfp ORF was excised from error-free pJet1.2-egfp with NheI and SphI and subcloned into NheI/SphI-digested pFastBacDUAL (Invitrogen), to generate plasmid pFB-egfp. An expression cassette containing the egfp reporter gene under transcriptional control of the very late p10 promoter was transposed from pFB-egfp into polyhedrin locus of vp80-null bacmid as described in the Bac-to-Bac manual (Invitrogen). In the resulting genome, the complete vp80 ORF has been removed (see FIG. 2). This corresponds to the deletion of 2074 bp from nucleotide positions 89564 to 91637 in the AcMNPV clone C6 genome provided in SEQ ID NO: 1.

Construction of Repaired Vp80-Null Bacmids

[0151] To prepare vp80 repair donor vectors, we modified plasmid pFB-egfp (noted above) by removing the polyhedrin promoter and replacing it with a fragment containing the vp80 promoter region and the vp80 ORF. First, a 2300-bp fragment containing both the vp80 promoter and ORF sequence was amplified using primers pvp80-StuI-F and vp80-XbaI-R (Table 1) from bacmid bMON14272 template, and cloned into vector pJet1.2/Blunt (Fermentas) to form pJet1.2-pvp80-vp80. After DNA sequence verification, the vp80 cassette was excised from pJet1.2-pvp80-vp80 by StuI/XbaI double digestion, and then subcloned into Bst1107I/XbaI-digested and gel-purified pFB-egfp to generate donor plasmid pFB-egfp-pvp80-vp80. Parallelly, a donor plasmid pFB-egfp-polh-vp80, where vp80 ORF is driven by the very late polyhedrin promoter (polh) was constructed. To this aim, a 2105-bp fragment carrying the vp80 ORF was amplified using primers vp80-SacI-F and vp80-XbaI-R (Table 1) and cloned into pJet1.2/Blunt, to generate pJet1.2-vp80. In the final step, the vp80 ORF was cut out (SacI/XbaI) from pJet1.2-vp80, and subcloned into SacI/XbaI-digested pFB-egfp, to create pFB-egfp-poIH-vp80.

[0152] To overcome a problem associated with the unavailability of anti-VP80 antibody, FLAG tag decoration (N- and C-terminus fusion) of VP80 was performed to facilitate immunodetection. The N-terminally fused FLAG-vp80 sequence was generated by a double-step PCR strategy, a so-called fusion PCR. First, a 259-bp fragment containing the vp80 promoter and the FLAG tag was PCR amplified using primers pvp80-StuI-F and vp80-FLAG-R1 from the bMON14272 bacmid template. After gel-purification and DNA quantification, the 259-bp fragment was used as forward primer in a second step PCR amplification with the reverse primer vp80-XbaI-R on the bMON14272 bacmid template. The final PCR product (2324 bp) was cloned into vector pJet1.2/Blunt (Fermentas) to form pJet1.2-pvp80-FLAG-vp80. After DNA sequence verification, the FLAG-vp80 cassette was excised from pJet1.2-pvp80-FLAG-vp80 by StuI/XbaI double digestion, and then subcloned into Bst1107I/XbaI-digested and gel-purified pFB-egfp to generate donor plasmid pFB-egfp-pvp80-FLAG-vp80. The C-terminally fused vp80-FLAG cassette was amplified using pvp80-StuI-F and vp80-FLAG-R from the bMON14272 bacmid template. The 2324-bp fragment was cloned into pJet1.2/Blunt, and subsequently transferred into pFB-egfp in a similar way as previous constructs.

[0153] The inserts of all developed donor plasmids were transposed into the vp80-null bacmid following the Bac-to-Bac protocol (Invitrogen). Screening of transposition-positive constructs into the polh locus was done by a triplex PCR-based assay employing M13 forward and reverse primers and a gentamicin resistance gene-specific primer GenR (Table 1).

Transfection-Infection Assay

[0154] Bacmid DNAs were prepared from 1.5-ml overnight bacterial cultures of 2 to 3 independent colonies carrying the bacmid with the inserted heterologous gene according to the Bac-to-Bac manual (Invitrogen) and were analyzed in parallel. For transfections, 1 .mu.g of each bacmid DNA preparation was used to transfect 1.times.10.sup.6 Sf9 cells in a 6-well plate by the Cellfectin.TM.-based transfection protocol as described in the Bac-to-Bac (Invitrogen) manual. From 72 h to 120 h post transfection (p.t.), viral propagation was checked by fluorescence microscopy. At 120 h p.t., the cell culture medium was centrifuged for 5 min at 2000.times.g to remove cell debris, and this clarified supernatant was used to infect 1.5.times.10.sup.6 Sf9 cells in 6-well plates. After 72 h p.i., the spread of virus infection was again monitored by fluorescence microscopy. In all experiments, a wild-type bMON14272 bacmid carrying the egfp reporter gene under control of the p10 promoter was used as positive control. A bMON14272-gp64null bacmid also carrying the egfp reporter gene under control p10 promoter served as negative control, since it has lost the ability of cell-to-cell movement of the infection (Lung et al., 2002).

Time-Course Characterization of Viral Propagation in Cell Culture

[0155] Time course analyses were performed to compare budded virus production of the AcMNPV-vp80null virus and the various repair constructs in comparison to the wild type AcMNPV bacmid (Ac-wt) all containing egfp. Briefly, the Sf9 cells were seeded in 6-well tissue culture plates (1.times.10.sup.6 cells/well in 1 ml Sf900-II culture medium without serum at 28.degree. C.). After two hours, the culture medium was removed, and the cells were transfected with 5 .mu.g bacmid DNA, under standard conditions as recommended in Bac-to-Bac manual (Invitrogen). Cell culture supernatants were harvested at 24, 48, 72, 96 and 120 h p.t., and analysed for the production of infectious budded virus by an end-point dilution assay to determine the tissue culture infective dose 50 (TCID.sub.50). Infection was determined by monitoring egfp expression (from the p10 promoter). The average values of infectious titers derived from three independent transfections were calculated and plotted into graphs.

Transmission Electron Microscopy

[0156] Insect Sf9 cells were seeded in a 25T flask (3.5.times.10.sup.6 cells/flask), and transfected with 20 .mu.g either the Ac-.DELTA.vp80, rescue Ac-.DELTA.vp80-vp80 or Ac-wt bacmid construct. After 48 h p.t., the cells were harvested and prepared for transmission electron microscopy as described previously (van Lent et al., 1990). Samples were examined and photographed with a Philips CM12 electron microscope.

Budded Virus Production Assay

[0157] Insect Sf9 cells were seeded in two 25T flasks (3.5.times.10.sup.6 cells/flask), and transfected with 20 .mu.g either Ac-.DELTA.vp80, Ac-.DELTA.vp80-vp80, Ac-.DELTA.vp80-pH-vp80, Ac-.DELTA.vp80-FLAG-vp80, Ac-.DELTA.vp80-vp80-FLAG, or Ac-wt bacmid construct. Five days p.t., the BV-enriched cell culture supernatants were harvested, and ultracentrifuged through a cushion of 10% sucrose solution (25,000 rpm for 1.5 hour, Beckman SW32). Pelleted budded virions were resuspended in sterile demi-water, and prepared for either negative staining electron microscopy, SDS-polyacrylamide electrophoresis, or PCR-based detection (as mentioned above).

Purification of ODVs and Rod-Shaped Structures from Infected Cells

[0158] The presence of ODVs and rod-like structures in infected/transfected insect cells was analyzed by electron microscopy (EM). For this purpose, insect cells were harvested 48 h p.i., lysed and the cell lysates were ultracentrifuged through a 40% sucrose cushion in TE (1 mM Tris-HCl pH 7.4, 0.1 mM EDTA) buffer (45,000 rpm for 1 hour, Beckman SW55). Pellets were resuspended in sterile demi-water and analyzed by negative staining EM as described previously (van Lent et al., 1990).

Purification and Fractionation of BV and ODV Virions

[0159] To produce BVs, 3.0.times.10.sup.7 Sf9 cells were infected with Ac-.DELTA.vp80-Flag.vp80 or control Ac-wt virus at an MOI=1. Six days p.i., 72 ml of BV-enriched medium was collected and centrifuged at 1,500.times.g for 10 min. The supernatant was then ultracentrifuged at 80,000.times.g (Beckman SW28 rotor) for 60 min at 4.degree. C. The BV pellet was resuspended in 350 .mu.l 0.1.times.TE buffer, and loaded onto a linear sucrose gradient (25 to 56% (w/v)), and ultracentrifuged at 80,000.times.g (Beckman SW55 rotor) for 90 min at 4.degree. C. The formed BV band was collected and diluted in 12 ml 0.1.times.TE. The BV preparation was concentrated at 80,000.times.g for 60 min at 4.degree. C. The final virus pellet was resuspended in 150 .mu.l of 0.1.times.TE.

[0160] To produce ODVs, 6.0.times.10.sup.7 Sf9 cells were co-infected with Ac-.DELTA.vp80-Flag.vp80 (MOI=25) and AcMNPV (MOI=5) viruses (strain E2, Smith & Summers, 1979). Five days p.i., the infected cells were harvested, and ODVs were purified from viral occlusion bodies as described previously (Braunagel et al., 1994). The final ODV pellet was resuspended in 0.5 ml of 0.1.times.TE (10 mM Tris, 1 mM EDTA, pH=7.5).

[0161] The purified BV and ODV virions were fractionated into envelope and nucleocapsid fractions as described previously (Braunagel et al., 1994). Final fractions were processed for SDS-PAGE and immunoblotted against either mouse monoclonal anti-Flag antibody (Stratagene), rabbit polyclonal anti-VP39 antiserum (kindly provided by Lorena Passarelli, Kansas State University, USA), rabbit polyclonal anti-GP64 antiserum (kindly provided by Hualin Wang and Feifei Yin, Wuhan Institute of Virology, China (Yin et al., 2008)), or rabbit polyclonal antiserum against per os infectivity factor 1 (PIF-1) (kindly provided by Ke Peng, Wageningen University, The Netherlands (Peng et al., 2010)).

Development of Transgenic Sf9-Derived Cell Line Expressing Vp80

[0162] To develop a cell line, which produces the VP80 protein, a 2105-bp fragment carrying the vp80 ORF was amplified using primers vp80-SacI-F and vp80-XbaI-R (Table 1) and cloned into pJet1.2/Blunt, to generate pJet1.2-vp80. In the next step, the vp80 ORF was cut out (SacI/XbaI) from pJet1.2-vp80, and subcloned into SacI/XbaI-digested pIZ (Invitrogen), to create pIZ-vp80. The resulting plasmid vector pIZ-vp80 was linearized with Eco57I, and gel-purified. Sf9 cells were seeded in a six-well plate (1.times.10.sup.6 cells/well), and transfected with 10 .mu.g of the linearized vector. After 24 hours post-transfection, cells were selected by cell culture medium containing Zeocin.TM. (300 .mu.g/ml) for 2 to 3 weeks, until no control Sf9 cells survived under the same conditions. Cells were then propagated as an uncloned cell line.

Recombinant Protein Expression with the vp80null Virus

[0163] To measure the capacity to express recombinant protein with the Ac-.DELTA.vp80 (trans-complemented) virus seed, 3.0.times.10.sup.7 non-transformed Sf9 cells were infected (independent triplicate assay) with Ac-wt, Ac-.DELTA.vp80-Flag.vp80 (both produced in non-transformed cell line) or Ac-.DELTA.vp80 virus (produced in the Sf9-vp80 cell line) at a MOI=10. All of these virus seeds are expressing egfp as a model heterologous gene from the baculovirus very late p10 promoter. At 48 h and 72 h p.i. cells and culture medium were harvested and used for Western blotting, enzyme-linked immunosorbent assay (ELISA) or BV titration (see above). For Western blotting the same antibodies as mentioned above were used to detect the Flag-tag, EGFP, and GP64, as well as a monoclonal mouse anti-actin antibody (ImmunO).

[0164] For relative quantification, Maxisorp 96-well plates (Nunc) were coated overnight at 4.degree. C. with 100 ng of rabbit polyclonal anti-GFP antibody (Molecular Probes) in a volume of 100 .mu.l per well, which was followed by standard ELISA procedures as previously described (Fric et al., 2008). The percentage of EGFP production was calculated (independent triplicate assay) according to the formula: % EGFP expression=(test absorbance.sub.nh-background absorbance)/(Ac-wt EGFP.sub.72h-background absorbance).times.100%, where nh represents the time point p.i. The statistical significance of the observed differences between the control Ac-wt and the experimental Ac-.DELTA.vp80-Flag.vp80 and Ac-.DELTA.vp80 genotypes was analyzed with the Student's t-test.

Results

The AcMNPV Vp80 Gene is Essential for Viral Replication

[0165] An AcMNPV deletion virus was constructed as detailed in FIG. 2. Repair constructs were designed such that the wild-type vp80 ORF or N- and C-terminally FLAG-tagged vp80 genes along with its native or polyhedrin promoter regions were inserted into the polyhedrin locus along with the egfp gene under the p10 promoter (FIG. 3A). To investigate the function of the vp80 gene, Sf9 cells were transfected with either the knock-out or repair bacmid constructs and monitored for EGFP expression by fluorescence microscopy. When Ac-vp80 null was introduced into Sf9 cells, no viral propagation was observed in cell culture at 72 h to 120 h p.t. We could observe only a "single-cell infection" phenotype similar to the phenotype of Ac-gp64null bacmid (FIG. 3B). The results indicate that Ac-vp80null is able to reach the very late phase of infection as confirmed by p10 promoter-driven EGFP expression. From 72 h to 120 hours p.t., widespread EGFP expression could be seen in insect cell monolayers that were transfected with the three repair (vp80 driven from its native promoter, vp80 driven from polyhedrin promoter and N-terminally FLAG-tagged vp80 driven from its native promoter) constructs indicating that these bacmids were able to produce levels of infectious budded virions sufficient to initiate secondary infection at a similar level as the wild-type bacmid (FIG. 3B). In contrast, in insect cells transfected with C-terminally FLAG-tagged vp80 repair constructs, by 72 h p.t. EGFP expression was only observed in isolated cells that were initially transfected indicating that this bacmid construct is defective in viral replication (FIG. 3B). However, by 96 h p.t. formation of tiny plaques was observed and by 120 h p.t. very few plaques of normal size were developed. The results show that the C-terminally flagged mutant is strongly delayed in producing budded virus and showed that an unmodified C-terminus is very important for the function of VP80. At 5 days p.t., cell culture supernatants were removed and added to freshly plated Sf9 cells and then incubated for 3 days to detect infection by virus generated from cells transfected with these bacmids. As expected, Sf9 cells incubated with supernatants from the transfections with repair constructs showed numerous EGFP expressing cells (FIG. 3C). Nevertheless, cells incubated with supernatants from C-terminally FLAG-tagged constructs showed a significant reduction in the number of EGFP-positive cells. On the other hand, in insect cells incubated with supernatants from the transfection with the vp80 knockout, no EGFP expression was detected at any time-point analyzed up to 72 h (FIG. 3C).

[0166] Moreover, to characterize the exact effect of deletion of the vp80 gene on AcMNPV infection, the viral propagation in transfected Sf9 cells was compared between Ac-wt, Ac-.DELTA.vp80, Ac-.DELTA.vp80-vp80Rep, Ac-.DELTA.vp80-polh-vp80Rep, Ac-.DELTA.vp80-FLAG-vp80Rep and Ac-.DELTA.vp80-vp80-FLAGRep. Cell culture supernatants of all the above bacmid constructs were analysed at indicated time points for BV production (FIG. 4). As expected, the repaired Ac-.DELTA.vp80-vp80Rep, Ac-.DELTA.vp80-polh-vp80Rep, and Ac-.DELTA.vp80-FLAG-vp80Rep viruses showed kinetics of viral replication consistent with wild-type virus (Ac-wt) propagation. Budded virion production by the C-terminally flagged Ac-.DELTA.vp80-vp80-FLAGRep virus was reduced to approximately 0.06% compared to the Ac-wt virus or the other repaired viruses.

[0167] These results indicate that the vp80 gene is essential for infectious BV production. It has clearly been proven that the whole sequence of vp80 ORF can completely be deleted from the bacmid backbone and adequately rescued by introduction of the vp80 ORF into a heterologous site (polyhedrin locus) of the genome. We also showed that vp80 gene expression can be driven by the heterologous polyhedrin promoter sequence with no negative effect on viral replication in cell culture. Additionally, we observed that the N-terminus in contrast to the C-terminus of VP80 is permissive to gene modifications (epitope tag-labeling). We noted that the kinetics of the C-terminally FLAG-tagged VP80 virus were significantly delayed when compared with all other rescue or wild-type viruses, indicating the functional importance of the VP80 C-terminus.

VP80 is Required for Production of Both BV and ODV

[0168] The results described above indicated that the Ac-vp80null mutant is completely defective in production of infectious budded virus. However, there was also a possibility that the mutant can still produce non-infectious budded particles. To investigate the ability, Sf9 cells were transfected with either the knock-out, repair or wild-type bacmid constructs and 7 days p.t. cell culture mediums were ultracentrifuged to pellet budded viruses. The formed pellets were either analyzed by negative staining electron microscopy or by Western blot- and PCR-based detection to confirm the presence of the budded viruses. No intact budded virus, virus-like particles, nor its structures (such as major capsid protein VP39 and viral genome sequence) were revealed in the pellet from the cells transfected with the Ac-vp80null mutant (FIGS. 5A and 5B). On the other hand, all analyzed repair constructs produced normally-appearing budded virus as compared with budded virus-derived from the wild-type virus (FIG. 5A). Nevertheless, it was very difficult to find representative budded virions in the pellet derived from C-terminally FLAG-tagged vp80 gene repair construct-transfected cells.

[0169] To further characterize deletion of the vp80 gene on baculovirus life cycle, electron microscopy was performed with ultra-thin sections generated from bacmid-transfected cells. The Ac-vp80null-transfected cells developed typical phenotypes of baculovirus-infected cells with an enlarged nucleus, a fragmented host chromatin, an electron-dense virogenic stroma, etc. (FIG. 6A). The absence of VP80 did not prevent formation of normally-appearing nucleocapsids inside the virogenic stroma (FIG. 6C). The formed nucleocapsids were phenotypically undistinguishable from those produced by either the Ac-vp80null repair or Ac-wt bacmids. However, an abundance of assembled nucleocapsids was rather less as compared with cells transfected with the Ac-vp80null repair or Ac-wt bacmids (FIGS. 6E and 6G). In addition, no occlusion-derived virions nor bundles of nucleocapsids prior to an envelopment could be observed in the peristromal compartment of a nucleoplasm (so called the ring zone) of Ac-vp80null bacmid-transfected cells (FIGS. 6B and 6D). It seems that VP80 plays a role during maturation of nucleocapsids and/or their release/transport from the virogenic stroma. Eventually, VP80 can somehow contribute to an efficient nucleocapsid assembly which could be explained by the small number of nucleocapsids present in the virogenic stroma of Ac-vp80null transfected cells. When the vp80 gene was re-introduced back into the bacmid mutant, a lot of nucleocapsids and occlusion-derived virions could be seen in the ring zones of transfected cells (FIG. 6F). An abundance and morphology of occlusion-derived virions produced in Ac-.DELTA.vp80-vp80 repair bacmid-transfected cells were similar to those produced by wild-type bacmid (FIGS. 6F and 6H).

VP80 is Associated with Nucleocapsids of Both BV and ODV

[0170] To investigate the association of VP80 with BV preparations, BVs were collected at 48 h p. i. and nucleocapsid and envelope fractions were separated. The Flag.VP80 protein was only detected in the nucleocapsid fraction as a double-band of molecular masses ranging between 80-kDa and 95-kDa that were observed in infected Sf9 cells (FIG. 14A, upper panel). Correct separation into nucleocapsid and envelope fractions was confirmed with antibodies against VP39 (nucleocapsid only) and GP64 (envelope only) (FIG. 14A, lower panels).

[0171] To examine whether VP80 is also associated with ODVs, Sf9 cells were co-infected with the Ac-.DELTA.vp80-Flag.vp80 and occlusion body (OB)-producing wt AcMNPV viruses to provide the POLH protein. Western blot analysis showed that VP80 associates with the nucleocapsid fraction of ODVs and in this case migrates as a single band of .about.80 kDa, corresponding to the 80-kDa form produced in the very late phase of infection (FIG. 14B, upper panel). Proper fractionation into nucleocapsid and envelope fractions was controlled with antiserum against PIF-1, an ODV envelope protein (FIG. 14B, lower panel).

The Function of VP80 can be Rescued by Genetic Trans-Complementation

[0172] To verify whether a vp80 deletion in the viral genome can be complemented by a vp80 ORF offered in trans under control of a constitutive promoter, a transgenic cell line expressing Flag-tagged vp80 was constructed. In these cells VP80 was mainly produced as a protein of approximately 95-kDa as was shown by Western blot analysis with anti-Flag antibody (FIG. 15A). Two minor bands, one of .about.80-kDa and a second of .about.65-kDa were also observed.

[0173] In trans-complementation assays, Sf9-vp80 cells were transfected with the Ac-.DELTA.vp80 bacmid, and the spread of virus infection was monitored by EGFP-specific fluorescence at 96 h and 120 h p.t. (FIG. 15Ba-c). Viral plaques were seen in the transfected Sf9-vp80 cells demonstrating that the virus was transmitted from cell to cell. Nevertheless, we noted that the number and size of the developed plaques was significantly smaller than observed in Sf9 cells transfected with the Ac-wt bacmid (FIG. 15d). As a control, non-transgenic Sf9 cells showed only single-cell infections when transfected with the Ac-.DELTA.vp80 bacmid (FIG. 15Bc).

[0174] When the culture medium of the Ac-.DELTA.vp80 transfected Sf9-vp80 cells was used to infect freshly seeded non-transgenic Sf9 cells a "single-cell infection" phenotype was observed (FIG. 15Bb, right panel). Hence, the BV particles resulting from trans-complementation were able to enter cells but were defective in producing new BV. This also shows that the Ac-.DELTA.vp80 did not revert to Ac-wt in the Sf9-vp80 cells, by picking up the transgene from the host cells. As predicted, no EGFP signal was detected in Sf9 cells receiving the supernatant from Ac-.DELTA.vp80-transfected, non-transgenic Sf9 cells (FIG. 15Bc, right panel). The numbers of infectious BVs released from the Sf9-vp80 cells transfected with the Ac-.DELTA.vp80 bacmid were compared with those produced in Sf9 cells transfected with Ac-wt at 6 days p.i. This experiment showed that the current trans-complementation system is approximately 25 fold less effective in BV production than the classical Sf9-based production system (FIG. 15C).

Trans-Complemented, Replication-Deficient Ac-vp80null Virus is Competent to Express High Levels of Recombinant Protein

[0175] To assess the effect of the vp80 gene deletion on the level of recombinant protein expression, a bench-scale comparative production assay has been performed. Herein, the Sf9 cells were in parallel infected with three types of baculovirus seeds at an MOI=10, namely (i) Ac-wt, (ii) Ac-.DELTA.vp80-Flag.vp80 (both produced in Sf9 cells), and (iii) Ac-.DELTA.vp80 (produced in Sf9-vp80 cells) all encoding EGFP. Western blotting profiles showed that the EGFP protein was expressed at identical levels for all three tested baculovirus genotypes as was the GP64 glycoprotein which served here for control purposes (FIG. 16A, upper panel). The relative amount of EGFP was quantified by ELISA at 48 and 72 h p.i. in infected cell lysates (FIG. 16B) and did not reveal any statistically significant difference in EGFP levels between the three tested baculovirus genotypes. The results thus demonstrate that the trans-complemented Ac-.DELTA.vp80 virus seed, although defective in viral replication, is as capable to produce recombinant protein as conventional baculovirus expression vectors as long as the initial multiplicity of infection is high enough to infect all cells.

[0176] Also during the production culture, revertant virus genotypes carrying the vp80 gene were not detected, as no de novo expressed Flag.VP80 protein (FIG. 16A) was detected in immunoblots. Theoretically, a certain quantity of Flag.VP80 protein associated with the trans-complemented virus seed is entering the insect cells, but this was no longer detected at very late times post-infection and is probably degraded by either lysosome- or proteasome-mediated activity. In the same experiment, no BV release was recorded in cell culture supernatants originated from Sf9 cells inoculated with the Ac-.DELTA.vp80 virus seed (FIG. 16C), demonstrating that neither revertant virus generation nor wild-type virus contamination had occurred.

Summary

[0177] In this study we focused on the improvement of conventional baculovirus-based expression tools with the goal to eliminate contaminating baculovirus progeny from manufactured recombinant protein(s). This effort is strongly driven by pharmaceutical perspectives, since recombinant baculovirus-expressed therapeutics are being more and more used in human and veterinary medicine. Hence, we aimed to identify baculovirus gene(s) whose targeting results in a deficiency of baculovirus virion production, but does not or only mildly affects very late gene expression. In this way high level expression of heterologous genes will be safeguarded.

[0178] A summarizing overview of the new technology with the vp80 gene as example is presented in FIG. 16. Using bacmid-based engineering the inventors constructed an AcMNPV genome lacking the vp80 gene (FIG. 16B). Functional genomics and electron microscopy analyses revealed that vp80 deficiency prevents production of both BVs and ODVs. In parallel, Sf9 cells were engineered to produce VP80 to trans-complement the Ac-.DELTA.vp80 knock-out bacmid (FIG. 14A,C). Finally, we proved that trans-complemented, replication-deficient baculovirus seed is capable of producing an amount of recombinant protein similar to that produced by conventional baculovirus vectors (FIG. 14D).

TABLE-US-00001 TABLE 1 List of PCR primers in order of appearance in the text. SEQ ID Orien- # Primer name Sequence tation 2 vp39-F 5'-gcttctaatacgactcactatagggtcgtatccgctaagcgttct-3' Forward 3 vp39-R 5'-gcttctaatacgactcactatagggacgcaacgcgttatacacag-3' Reverse 4 45510 5'-gcttctaatacgactcactatagggacagcgtgtacgagtgcat-'3 Forward 5 46235 5'-gcttctaatacgactcactatagggatctcgagcgtgtagctggt-3' Reverse 6 90292 5'-gcttctaatacgactcactatagggtaccgccgaacattacacc-3' Forward 7 90889 5'-gcttctaatacgactcactatagggtctattggcacgtttgct-3' Reverse 8 ec-27-F 5'-gcttctaatacgactcactatagggaaagcagacactcggcagat-3' Forward 9 ec-27-R 5'-gcttctaatacgactcactatagggttgagtggcttcaacctcag-3' Reverse 10 dbp-F 5'-gcttctaatacgactcactatagggcgctcgctagttttgttct-3' Forward 11 dbp-R 5'-gcttctaatacgactcactatagggaaagatcggaaggtggtga-3' Reverse 12 gfp-F 5'-gcttctaatacgactcactatagggctgaccctgaagttcatctg-3' Forward 13 gfp-R 5'-gcttctaatacgactcactatagggaactccagcaggaccatgt-3' Reverse 14 cat-F 5'-gcttctaatacgactcactatagggacggcatgatgaacctgaat-3' Forward 15 cat-R 5'-gcttctaatacgactcactatagggatcccaatggcatcgtaaag-3' Reverse 16 vp80-ko-F 5'-ctgtattgtaatctgtaagcgcacatggtgcattcgatataaccttataatgtgt- Forward gctggaatgccct-3' 17 vp80-ko-R 5'-aaatgtactgaatataaataaaaattaaaaatattttataattttttatttaccgtt- Reverse cgtatagcatacat-3' 18 89507 5'-agcggtcgtaaatgttaaacc-3' Forward 19 91713 5'-tgtataaacaatatgttaatatgtg-3' Reverse 20 gfp-NheI-F 5'-ccaaaccgctagcaacatggtgagcaagggcgag-3' Forward 21 gfp-SphI 5'-aggaaagggcatgcttaacgcgtaccggtcttgtacagctcgtccatgc-3' Reverse 22 pvp80-StuI-F 5'-ggaacaaaggcctgagctcaaagtaagacctttactgtcc-3' Forward 23 vp80-XbaI-R 5'-ccttctatctagattatataacattgtagtttgcg-3' Reverse 24 vp80-SacI-F 5'-ttatcttgagctcaatatgaacgattccaattctc-3' Forward 25 vp80-FLAG-R1 5'-caacagagaattggaatcgttcttatcgtcgtcatccttgtaatc- Reverse catattataaggttatatcgaatg-3' 26 vp80-FLAG-R 5'-ccttctatctagattacttatcgtcgtcatccttgtaatctataacat- Reverse tgtagtttgcgttc-3' 27 M13-F 5'-cccagtcacgacgttgtaaaacg-3' Forward 28 M13-R 5'-agcggataacaatttcacacagg-3' Reverse 29 GenR 5'-agccacctactcccaacatc-3' Reverse 30 vp39-ko-F 5'-cttcttatcgggttgtacaac-3' Forward 31 vp39-ko-R 5'-gcgtatcatgacgatggatg-3' Reverse 32 vp39-SacI-F 5'-aaggttctctagattagacggctattcctccac-3' Forward 33 vp39-XbaI-R 5'-ttatcttgagctcaatatggcgctagtgcccg-3' Reverse 34 vp39-StuI-F 5'-ggaacaaaggcctgagctcttagacggctattcctccac-3' Forward 35 lef-4-XbaI-R 5'-ccttctatctagattaatttggcacgattcggtc-3' Reverse 36 cg-30-XbaI-F 5'-aaggttctctagattaatctacatttattgtaacatttg-3' Forward 37 vp39-FLAG-SacI- 5'-ttatcttgagctcaatatggattacaaggatgacgacgataaggc- Reverse R gctagtgcccgtgggt-3' 38 vp1054-ko-F 5'-gtactgaaagataatttatttttgatagataataattacattattttaa- Forward acgtgttcgaccaagaaaccgat-3' 39 vp1054-ko-R1 5'-agggcgaattccagcacactttattacgtggacgcgttactttgc-3' Reverse 40 vp1054-ko-R2 5'-gataagaatgcttgtttaacaaataggtcagctgttaaatact- Reverse ggcgatgtaccgttcgtatagcatacat-3' 41 vp1054-Rep-F 5'-ggttgtttaggcctgagctcctttggtacgtgttagagtgt-3' Forward 42 vp1054-Rep-R 5'-tcctttcctctagattacacgttgtgtgcgtgcaga-3' Reverse 43 p6.9-ko-F 5'-gcttcgttcattcgctactgtcggctgtgtggaatgtctggttgtt- Forward aagtgtgctggaattcgccct-3' 44 p6.9-ko-R 5'-aatattaataaggtaaaaattacagctacataaattacacaattta- Reverse aactaccgttcgtatagcatacat-3' 45 Ac-p6.9-F 5'-tttgaattcatggttgcccgaagctccaagac-3' Forward 46 Ac-p6.9-R 5'-tttgcggccgcttaatagtagcgtgttctgtaac-3' Reverse 47 Se-p6.9-F 5'-tttgaattcatgtatcgtcgtcgttcatc-3' Forward 48 Se-p6.9-R 5'-tttgcggccgcttaatagtggcgacgtctgtatc-3' Reverse 49 86596 5'-gggcttagtttaaaatcttgca-3' Forward 50 86995 5'-aattcaaacgaccaagacgag-3' Reverse 51 45122 5'-gcaatcatgacgaacgtatgg-3' Forward 52 46441 5'-cgataatttttccaagcgctac-3' Reverse 53 pp6.9-F 5'-ggtcgacgtaccaaattccgttttgcgacg-3' Forward 54 pp6.9-R 5'-ggtcgacggatccgtttaaattgtgtaatttatg-3' Reverse 55 75834 5'-cttcttatcgggttgtacaac-3' Forward 56 76420 5'-gcgtatcatgacgatggatg-3' Reverse

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Sequence CWU 1

1

561133894DNAAutographa californica nucleopolyhedrovirus 1gaattctacc cgtaaagcga gtttagtttt gaaaaacaaa tgacatcatt tgtataatga 60catcatcccc tgattgtgtt ttacaagtag aattctatcc gtaaagcgag ttcagttttg 120aaaacaaatg agtcatacct aaacacgtta ataatcttct gatatcagct tatgactcaa 180gttatgagcc gtgtgcaaaa catgagataa gtttatgaca tcatccactg atcgtgcgtt 240acaagtagaa ttctactcgt aaagccagtt cggttatgag ccgtgtgcaa aacatgacat 300cagcttatga ctcatacttg attgtgtttt acgcgtagaa ttctactcgt aaagcgagtt 360cggttatgag ccgtgtgcaa aacatgacat cagcttatga gtcataatta atcgtgcgtt 420acaagtagaa ttctactcgt aaagcgagtt gaaggatcat atttagttgc gtttatgaga 480taagattgaa agcacgtgta aaatgtttcc cgcgcgttgg cacaactatt tacaatgcgg 540ccaagttata aaagattcta atctgatatg ttttaaaaca cctttgcggc ccgagttgtt 600tgcgtacgtg actagcgaag aagatgtgtg gaccgcagaa cagatagtaa aacaaaaccc 660tagtattgga gcaataatcg atttaaccaa cacgtctaaa tattatgatg gtgtgcattt 720tttgcgggcg ggcctgttat acaaaaaaat tcaagtacct ggccagactt tgccgcctga 780aagcatagtt caagaattta ttgacacggt aaaagaattt acagaaaagt gtcccggcat 840gttggtgggc gtgcactgca cacacggtat taatcgcacc ggttacatgg tgtgcagata 900tttaatgcac accctgggta ttgcgccgca ggaagccata gatagattcg aaaaagccag 960aggtcacaaa attgaaagac aaaattacgt tcaagattta ttaatttaat taatattatt 1020tgcattcttt aacaaatact ttatcctatt ttcaaattgt tgcgcttctt ccagcgaacc 1080aaaactatgc ttcgcttgct ccgtttagct tgtagccgat cagtggcgtt gttccaatcg 1140acggtaggat taggccggat attctccacc acaatgttgg caacgttgat gttacgttta 1200tgcttttggt tttccacgta cgtcttttgg ccggtaatag ccgtaaacgt agtgccgtcg 1260cgcgtcacgc acaacaccgg atgtttgcgc ttgtccgcgg ggtattgaac cgcgcgatcc 1320gacaaatcca ccactttggc aactaaatcg gtgacctgcg cgtctttttt ctgcattatt 1380tcgtctttct tttgcatggt ttcctggaag ccggtgtaca tgcggtttag atcagtcatg 1440acgcgcgtga cctgcaaatc tttggcctcg atctgcttgt ccttgatggc aacgatgcgt 1500tcaataaact cttgtttttt aacaagttcc tcggtttttt gcgccaccac cgcttgcagc 1560gcgtttgtgt gctcggtgaa tgtcgcaatc agcttagtca ccaactgttt gctctcctcc 1620tcccgttgtt tgatcgcggg atcgtacttg ccggtgcaga gcacttgagg aattacttct 1680tctaaaagcc attcttgtaa ttctatggcg taaggcaatt tggacttcat aatcagctga 1740atcacgccgg atttagtaat gagcactgta tgcggctgca aatacagcgg gtcgcccctt 1800ttcacgacgc tgttagaggt agggccccca ttttggatgg tctgctcaaa taacgatttg 1860tatttattgt ctacatgaac acgtatagct ttatcacaaa ctgtatattt taaactgtta 1920gcgacgtcct tggccacgaa ccggacctgt tggtcgcgct ctagcacgta ccgcaggttg 1980aacgtatctt ctccaaattt aaattctcca attttaacgc gagccatttt gatacacgtg 2040tgtcgatttt gcaacaacta ttgtttttta acgcaaacta aacttattgt ggtaagcaat 2100aattaaatat gggggaacat gcgccgctac aacactcgtc gttatgaacg cagacggcgc 2160cggtctcggc gcaagcggct aaaacgtgtt gcgcgttcaa cgcggcaaac atcgcaaaag 2220ccaatagtac agttttgatt tgcatattaa cggcgatttt ttaaattatc ttatttaata 2280aatagttatg acgcctacaa ctccccgccc gcgttgactc gctgcacctc gagcagttcg 2340ttgacgcctt cctccgtgtg gccgaacacg tcgagcgggt ggtcgatgac cagcggcgtg 2400ccgcacgcga cgcacaagta tctgtacacc gaatgatcgt cgggcgaagg cacgtcggcc 2460tccaagtggc aatattggca aattcgaaaa tatatacagt tgggttgttt gcgcatatct 2520atcgtggcgt tgggcatgta cgtccgaacg ttgatttgca tgcaagccga aattaaatca 2580ttgcgattag tgcgattaaa acgttgtaca tcctcgcttt taatcatgcc gtcgattaaa 2640tcgcgcaatc gagtcaagtg atcaaagtgt ggaataatgt tttctttgta ttcccgagtc 2700aagcgcagcg cgtattttaa caaactagcc atcttgtaag ttagtttcat ttaatgcaac 2760tttatccaat aatatattat gtatcgcacg tcaagaatta acaatgcgcc cgttgtcgca 2820tctcaacacg actatgatag agatcaaata aagcgcgaat taaatagctt gcgacgcaac 2880gtgcacgatc tgtgcacgcg ttccggcacg agctttgatt gtaataagtt tttacgaagc 2940gatgacatga cccccgtagt gacaacgatc acgcccaaaa gaactgccga ctacaaaatt 3000accgagtatg tcggtgacgt taaaactatt aagccatcca atcgaccgtt agtcgaatca 3060ggaccgctgg tgcgagaagc cgcgaagtat ggcgaatgca tcgtataacg tgtggagtcc 3120gctcattaga gcgtcatgtt tagacaagaa agctacatat ttaattgatc ccgatgattt 3180tattgataaa ttgaccctaa ctccatacac ggtattctac aatggcgggg ttttggtcaa 3240aatttccgga ctgcgattgt acatgctgtt aacggctccg cccactatta atgaaattaa 3300aaattccaat tttaaaaaac gcagcaagag aaacatttgt atgaaagaat gcgtagaagg 3360aaagaaaaat gtcgtcgaca tgctgaacaa caagattaat atgcctccgt gtataaaaaa 3420aatattgaac gatttgaaag aaaacaatgt accgcgcggc ggtatgtaca ggaagaggtt 3480tatactaaac tgttacattg caaacgtggt ttcgtgtgcc aagtgtgaaa accgatgttt 3540aatcaaggct ctgacgcatt tctacaacca cgactccaag tgtgtgggtg aagtcatgca 3600tcttttaatc aaatcccaag atgtgtataa accaccaaac tgccaaaaaa tgaaaactgt 3660cgacaagctc tgtccgtttg ctggcaactg caagggtctc aatcctattt gtaattattg 3720aataataaaa caattataaa tgctaaattt gttttttatt aacgatacaa accaaacgca 3780acaagaacat ttgtagtatt atctataatt gaaaacgcgt agttataatc gctgaggtaa 3840tatttaaaat cattttcaaa tgattcacag ttaatttgcg acaatataat tttattttca 3900cataaactag acgccttgtc gtcttcttct tcgtattcct tctctttttc atttttctcc 3960tcataaaaat taacatagtt attatcgtat ccatatatgt atctatcgta tagagtaaat 4020tttttgttgt cataaatata tatgtctttt ttaatggggt gtatagtacc gctgcgcata 4080gtttttctgt aatttacaac agtgctattt tctggtagtt cttcggagtg tgttgcttta 4140attattaaat ttatataatc aatgaatttg ggatcgtcgg ttttgtacaa tatgttgccg 4200gcatagtacg cagcttcttc tagttcaatt acaccatttt ttagcagcac cggattaaca 4260taactttcca aaatgttgta cgaaccgtta aacaaaaaca gttcacctcc cttttctata 4320ctattgtctg cgagcagttg tttgttgtta aaaataacag ccattgtaat gagacgcaca 4380aactaatatc acaaactgga aatgtctatc aatatatagt tgctgatatc atggagataa 4440ttaaaatgat aaccatctcg caaataaata agtattttac tgttttcgta acagttttgt 4500aataaaaaaa cctataaata tgccggatta ttcataccgt cccaccatcg ggcgtaccta 4560cgtgtacgac aacaagtact acaaaaattt aggtgccgtt atcaagaacg ctaagcgcaa 4620gaagcacttc gccgaacatg agatcgaaga ggctaccctc gaccccctag acaactacct 4680agtggctgag gatcctttcc tgggacccgg caagaaccaa aaactcactc tcttcaagga 4740aatccgtaat gttaaacccg acacgatgaa gcttgtcgtt ggatggaaag gaaaagagtt 4800ctacagggaa acttggaccc gcttcatgga agacagcttc cccattgtta acgaccaaga 4860agtgatggat gttttccttg ttgtcaacat gcgtcccact agacccaacc gttgttacaa 4920attcctggcc caacacgctc tgcgttgcga ccccgactat gtacctcatg acgtgattag 4980gatcgtcgag ccttcatggg tgggcagcaa caacgagtac cgcatcagcc tggctaagaa 5040gggcggcggc tgcccaataa tgaaccttca ctctgagtac accaactcgt tcgaacagtt 5100catcgatcgt gtcatctggg agaacttcta caagcccatc gtttacatcg gtaccgactc 5160tgctgaagag gaggaaattc tccttgaagt ttccctggtg ttcaaagtaa aggagtttgc 5220accagacgca cctctgttca ctggtccggc gtattaaaac acgatacatt gttattagta 5280catttattaa gcgctagatt ctgtgcgttg ttgatttaca gacaattgtt gtacgtattt 5340taataattca ttaaatttat aatctttagg gtggtatgtt agagcgaaaa tcaaatgatt 5400ttcagcgtct ttatatctga atttaaatat taaatcctca atagatttgt aaaataggtt 5460tcgattagtt tcaaacaagg gttgtttttc cgaaccgatg gctggactat ctaatggatt 5520ttcgctcaac gccacaaaac ttgccaaatc ttgtagcagc aatctagctt tgtcgatatt 5580cgtttgtgtt ttgttttgta ataaaggttc gacgtcgttc aaaatattat gcgcttttgt 5640atttctttca tcactgtcgt tagtgtacaa ttgactcgac gtaaacacgt taaataaagc 5700ttggacatat ttaacatcgg gcgtgttagc tttattaggc cgattatcgt cgtcgtccca 5760accctcgtcg ttagaagttg cttccgaaga cgattttgcc atagccacac gacgcctatt 5820aattgtgtcg gctaacacgt ccgcgatcaa atttgtagtt gagctttttg gaattatttc 5880tgattgcggg cgtttttggg cgggtttcaa tctaactgtg cccgatttta attcagacaa 5940cacgttagaa agcgatggtg caggcggtgg taacatttca gacggcaaat ctactaatgg 6000cggcggtggt ggagctgatg ataaatctac catcggtgga ggcgcaggcg gggctggcgg 6060cggaggcgga ggcggaggtg gtggcggtga tgcagacggc ggtttaggct caaatgtctc 6120tttaggcaac acagtcggca cctcaactat tgtactggtt tcgggcgccg tttttggttt 6180gaccggtctg agacgagtgc gatttttttc gtttctaata gcttccaaca attgttgtct 6240gtcgtctaaa ggtgcagcgg gttgaggttc cgtcggcatt ggtggagcgg gcggcaattc 6300agacatcgat ggtggtggtg gtggtggagg cgctggaatg ttaggcacgg gagaaggtgg 6360tggcggcggt gccgccggta taatttgttc tggtttagtt tgttcgcgca cgattgtggg 6420caccggcgca ggcgccgctg gctgcacaac ggaaggtcgt ctgcttcgag gcagcgcttg 6480gggtggtggc aattcaatat tataattgga atacaaatcg taaaaatctg ctataagcat 6540tgtaatttcg ctatcgttta ccgtgccgat atttaacaac cgctcaatgt aagcaattgt 6600attgtaaaga gattgtctca agctcggatc ccgcacgccg ataacaagcc ttttcatttt 6660tactacagca ttgtagtggc gagacacttc gctgtcgtcg acgtacatgt atgctttgtt 6720gtcaaaaacg tcgttggcaa gctttaaaat atttaaaaga acatctctgt tcagcaccac 6780tgtgttgtcg taaatgttgt ttttgataat ttgcgcttcc gcagtatcga cacgttcaaa 6840aaattgatgc gcatcaattt tgttgttcct attattgaat aaataagatt gtacagattc 6900atatctacga ttcgtcatgg ccaccacaaa tgctacgctg caaacgctgg tacaatttta 6960cgaaaactgc aaaaacgtca aaactcggta taaaataatc aacgggcgct ttggcaaaat 7020atctatttta tcgcacaagc ccactagcaa attgtatttg cagaaaacaa tttcggcgca 7080caattttaac gctgacgaaa taaaagttca ccagttaatg agcgaccacc caaattttat 7140aaaaatctat tttaatcacg gttccatcaa caaccaagtg atcgtgatgg actacattga 7200ctgtcccgat ttatttgaaa cactacaaat taaaggcgag ctttcgtacc aacttgttag 7260caatattatt agacagctgt gtgaagcgct caacgatttg cacaagcaca atttcataca 7320caacgacata aaactcgaaa atgtcttata tttcgaagca cttgatcgcg tgtatgtttg 7380cgattacgga ttgtgcaaac acgaaaactc acttagcgtg cacgacggca cgttggagta 7440ttttagtccg gaaaaaattc gacacacaac tatgcacgtt tcgtttgact ggtacgccgt 7500cggcgtgtta acatacaagt tgctaaccgg cggccgacac ccatttgaaa aaagcgaaga 7560cgaaatgttg gacttgaata gcatgaagcg tcgtcagcaa tacaatgaca ttggcgtttt 7620aaaacacgtt cgtaacgtta acgctcgtga ctttgtgtac tgcctaacaa gatacaacat 7680agattgtaga ctcacaaatt acaaacaaat tataaaacat gagtttttgt cgtaaaaatg 7740ccacttgttt tacgagtaga attctacgtg taacacacga tctaaaagat gatgtcattt 7800tttatcaatg actcatttgt tttaaaacag acttgtttta cgagtagaat tctacgtgta 7860aagcatgatc gtgagtggtg ttaataaaat cataaaaatt attgtaaatg tttattattt 7920aaaaacgatt caaatatata ataaaaacaa tctacatcta tttcttcaca atccataaca 7980cacaacaggt ccatcaatga gtttttgtct ttatccgaca tactatgtgc atgtaacaaa 8040tcaaatacat cttttaaatt tttatacaca tctttacatt gtctaccaaa atctttaata 8100accctataac aaggaaaaga cttttcttct tgcgtggttt tgccgcgcag atattgaaat 8160aaaatgtgca tgcacgacaa cttgtgttta ctaaaatgct ccttgcctat accgcaaaac 8220cggccataca tttcggcgat tacacgcgga caattgtacg attcgtctac gtgtaaacga 8280tcatcataat cactcttgcg caaacgaata aattttttca ccgcttccga caaacgaggc 8340accaattcgg cgggcacgct tcgatacatt attctgtgca cataagttac cacacaaaat 8400ttattgtacc accatccgac aacgtcgtta ttagggttga acacgttggc gatgcgcagc 8460agtttcccgt ttctcatgaa atattcaaag cggcccaaaa taatttgcaa gcaatccaac 8520atgtcttgag aaatttctcg ttcaaaattg ttcaaagaga atatctgcca tccgttttga 8580acgcgcacgc tgacgggaac caccgcatcg atttgctcca acacttcacg gacgttatcg 8640tcgatgccca tcgtttcgct ggtgctgaac caatgggaaa ggctcttgat ggaatcgccc 8700gcgtctatca tcttgaccgc ttcgtcaaag gtgcaactgc cgctcttcaa acgccgcata 8760gcggtcacgt cccgctctat gcacgacata ccgtttacgt acgattctga taggtattcc 8820tgaactatac ggtaatggtg atacgactcg ccatacacgt cgtgcacctc attgtattta 8880gcataataat tgtaaattat taactttgca gcgagagaca tgttgtcagt aaagcggtgc 8940taggctcaat aatactgatg tacaggcacg cgtgctattt atatataatt tcgcaaggag 9000gggagctgtt atcggttgct attattaaag aatggccgtc tgtttttatc acaagcttgg 9060cagcctcaac catgaagcgt cgtcattgta aattaaattc tctgcctcaa gaattatttg 9120acaagattgt cgagtattta tctttatctg attactgcaa tttggtgctt gtctgtaaaa 9180gaccttctag taaatataac gtgatatttg atagtactaa tcaccaacat ttgaaaggcg 9240tgtacaaaaa gacagacgtg caaataacaa gctacaacga atacatcaac tgtatttgca 9300acgaactgag acaagacgaa ttctatgcca aatcatcatg gattgcgagt atttgcggtc 9360accagagagc gacaattttt agtgtaacaa ataaacaagt agaaatgaaa tatcatttgt 9420ataatatagc aattgtggaa agtgaagatt gcaacggatt ttacccattt gagccaacgc 9480gcgattgttt aatatgcaaa caaaaaaacc aatgtcctcg taattcattt attgtttcgt 9540tgtgtaaata tttagaaaaa caaaatgtac aatcaaactt tatatattat ttatacgaaa 9600taaatacata ataataacta ttatacatgt ttttatttta caatacttcc tgtataacct 9660ctctaactac attaggagta caatccacgt caattacacg tttagctatt tttctaattt 9720tgtaatgttt atcgtagagt ttttcgttaa tacattgaat agccaacaag ggatttgggt 9780gcacaccgtc atagagtact tccatgtcgt cttcaaagcg catttttcgc ttgcgaaaat 9840gccgctcttg gcccaaaaca aaagcgagtt tgatgcggtc gtcgatgcgt tccgaaaata 9900cggccaaatg ctggtgtttg gtgatgtcgc gcggaaacgt caccgtgcca tttttgcttt 9960ccgccacgac ggcggttttc aatttttcgg ccgactgcag catgttaagt ttggcgtcga 10020gttcgtgcaa acgcaattca aactgctcaa acctgttgcc cacctcgttc ttgaacgtct 10080cgtgggtgac cataaatttt tcgctgtttg cattcagttt ctttacatgt tttaaaacag 10140attcaatctt gtcgcgcaaa tcatcacgct cgccttcagt ttgaatgtgc agcaacgcgt 10200tgcttttgtt ggcaaaattt aaccgcatca aaatttccaa caacccgtgc ttggtcgcga 10260acaatgcgcc caacgagttg agatcgcgtt tggatctctg tttgtgaaaa acaatttcgt 10320ttaaatggta aacttgatcg ccgtcccaat tgcaatcaag tatgtcgtcg tgcgcaattt 10380caagaccttt gcaaaaatct atcacattgt agcattttgc gttcgtgtcg ctgtgcacgt 10440atctgtactt gaaactgtgc gtgttgcatt tgaatgagtc ccatttaacg atgtgcgacc 10500attgttgggc gtttatgtgg tactttttgt agtcgtctgc attgaaccga tcttcggcgg 10560cgatggcgtc gttgtcgttg tcaccggacc acatccacca gttccataac caggatagca 10620ttgctttagc ttgtctagca attcctttgt tatacaacga gaaaatttcg ttcccttata 10680attatagctg tacggtgcgc gtatttgttt gttaacgtta caaaaaatat ccctgtccac 10740gtccggccaa tactgcaacg tgagcgcgtc caagtttgaa tcttgcatat gcggaacgta 10800caaacgtacg gcctctctca cacaatgcgc aaaactgccc ggctgaatgt aatcactgtc 10860caactttgca ggtttctcga aagccttgta ccgatgcacg cgaacatttt gagcggacgt 10920gattttaaac ttgtcggtga attttaacca caaatgaaat ccacggttgc cggtatacat 10980gactcttgac acgttctctt ccgtgtaaaa caacagaaac gccgtggcgc caatgtaaat 11040tttcagcatt aaatcgtgtt cgtcaacata atttttgtaa tcggcgtcta cgacccattc 11100cctgccgccg ccgtcgtcca acggtttgac gtgcacgtcg gacactttgt tttgcacaat 11160ataactatac aattgtgcgg aggtatcaaa atatctgtcg gcgtgaatcc agcgcgcgtt 11220gaccgtcatg aacgcgtact tgcggctgtc gttgtacgca atggcgtccc acatcatgtc 11280gacgcgcttc tgcgtataat tgcacactaa catgttgccc tttgaacttg acctcgattg 11340tgttaatttt tggctataaa aaggtcaccc tttaaaattt gttacataat caaattacca 11400gtacagttat tcggtttgaa gcaaaatgac tattctctgc tggcttgcac tgctgtctac 11460gcttactgct gtaaatgcgg ccaatatatt ggccgtgttt cctacgccag cttacagcca 11520ccatatagtg tacaaagtgt atattgaagc ccttgccgaa aaatgtcaca acgttacggt 11580cgtcaagccc aaactgtttg cgtattcaac taaaacttat tgcggtaata tcacggaaat 11640taatgccgac atgtctgttg agcaatacaa aaaactagtg gcgaattcgg caatgtttag 11700aaagcgcgga gtggtgtccg atacagacac ggtaaccgcc gctaactacc taggcttgat 11760tgaaatgttc aaagaccagt ttgacaatat caacgtgcgc aatctcattg ccaacaacca 11820gacgtttgat ttagtcgtcg tggaagcgtt tgccgattat gcgttggtgt ttggtcactt 11880gtacgatccg gcgcccgtaa ttcaaatcgc gcctggctac ggtttggcgg aaaactttga 11940cacggtcggc gccgtggcgc ggcaccccgt ccaccatcct aacatttggc gcagcaattt 12000cgacgacacg gaggcaaacg tgatgacgga aatgcgtttg tataaagaat ttaaaatttt 12060ggccaacatg tccaacgcgt tgctcaaaca acagtttgga cccaacacac cgacaattga 12120aaaactacgc aacaaggtgc aattgctttt gctaaacctg catcccatat ttgacaacaa 12180ccgacccgtg ccgcccagcg tgcagtatct tggcggagga atccatcttg taaagagcgc 12240gccgttgacc aaattaagtc cggtcatcaa cgcgcaaatg aacaagtcaa aaagcggaac 12300gatttacgta agttttgggt cgagcattga caccaaatcg tttgcaaacg agtttcttta 12360catgttaatc aatacgttca aaacgttgga taattacacc atattatgga aaattgacga 12420cgaagtagta aaaaacataa cgttgcccgc caacgtaatc acgcaaaatt ggtttaatca 12480acgcgccgtg ctgcgtcata aaaaaatggc ggcgtttatt acgcaaggcg gactacaatc 12540gagcgacgag gccttggaag ccgggatacc catggtgtgt ctgcccatga tgggcgacca 12600gttttaccat gcgcacaaat tacagcaact cggcgtagcc cgcgccttgg acactgttac 12660cgtttccagc gatcaactac tagtggcgat aaacgacgtg ttgtttaacg cgcctaccta 12720caaaaaacac atggccgagt tatatgcgct catcaatcat gataaagcaa cgtttccgcc 12780tctagataaa gccatcaaat tcacagaacg cgtaattcga tatagacatg acatcagtcg 12840tcaattgtat tcattaaaaa caacagctgc caatgtaccg tattcaaatt actacatgta 12900taaatctgtg ttttctattg taatgaatca cttaacacac ttttaattac gtcaataaat 12960gttattcacc attatttacc tggttttttt gagaggggct ttgtgcgact gcgcacttcc 13020agcctttata aacgctcacc aaccaaagca ggtcattatt gtgccaggac gttcaaaggc 13080gaaacatcga aatggagtct gttcaaacgc gcttatgtgc cagtagcaat caatttgctc 13140cgttcaaaaa gcgccagctt gccgtgccgg tcggttctgt gaacagtttg acacacacca 13200tcacctccac caccgtcacc agcgtgattc caaaaaatta tcaagaaaaa cgtcagaaaa 13260tatgccacat aatatcttcg ttgcgtaaca cgcacttgaa tttcaataag atacagtctg 13320tacataaaaa gaaactgcgg catttgcaaa atttgctaag aaaaaagaac gaaattattg 13380ccgagttggt tagaaaactt gaaagtgcac agaagaagac aacgcacaga aatattagta 13440aaccagctca ttggaaatac tttggagtag tcagatgtga caacacaatt cgcacaatta 13500ttggcaacga aaagtttgta aggagacgtt tggccgagct gtgcacattg tacaacgccg 13560agtacgtgtt ttgccaagca cgcgccgatg gagacaaaga tcgacaggca ctagcgagtc 13620tgctgacggc ggcgtttggt tcgcgagtca tagtttatga aaatagtcgc cggttcgagt 13680ttataaatcc ggacgagatt gctagtggta aacgtttaat aattaaacat ttgcaagatg 13740aatctcaaag tgatattaac gcctattaat ttgaaaggtg aggaagagcc caattgcgtt 13800gagcgcatta ccataatgcc atgtatttta atagatactg agatctgttt aaatgtcaga 13860tgccgttctc cttttgccaa attcaaagta ttgattattg tagatggctt tgatagcgct 13920tatattcagg ctaccttttg tagcattagc gatagtgtaa caattgttaa caaatctaac 13980gaaaagcatg taacgtttga cgggtttgta aggccggacg atgaaggtac aacaatgcct 14040tatgtcattg gaccattata ttctgtcgac gctgctgtcg ccgaccgtaa agtgaaggac 14100gtggtggatt caattcaaaa ccaacagaca atgttaaaag tatttattaa cgaggctaat 14160gtgtataaca aatggaatat gcttaaaggt ttaatttata ataataacaa tgaatctgtt 14220ttagtaaaat aatgtagtaa aatttataaa ggtagataaa aattataata ttaataaaaa 14280aaataatgtt actaaatggg ttcctgcgtt aaattatttt acgggtagac agctattaac 14340tattttattt atttttaaat ttaaataaat gtattgttag aaaattgtgt tgttttatta 14400gtataacgaa aaaatacatg acataaaccg cttccaattt tggtcacaca aactcttgtg 14460tggatagttt acgtaatgag ttaaataggc gggcagttgt ccgctaaacg tgtcggtggt 14520caagtagatg tgcattaatt tacgacaacc caaagcgggg ccgcttatgt caagtatttt 14580tttcacaaaa ttggtaatgg tttcgttttg ttccttgtac aaacacatgt cggtgtgatc 14640gttgacgcac gagttgtacg attccgccgg caggttggca aacaagcgct tgagatgctt 14700gagtctgcgt tcaattttat aatcaaactt gttggtgaaa atgtctttca gcaagcacat 14760taactggtcg ttcaaaacgc gctgcaacga cgacaccaac acatgatatt cgtttccaaa 14820aagcgaaaaa tttttgatgc agcggtccgc gttgaagggt cgtttcataa tgcgcacgtt 14880gacaaaaaac acgttgaaag acagcggggc tgtggttatt ttaacgccgt tgtcggtata 14940ctcgtcgacg ccgtctgcgc ttgttatgtc aatttgtagc gcaaatctaa ccaaatcaaa 15000ctcatcgttg

tactgtgtct ttatgcattt tatatggcgg tttaagtgca agttgatttg 15060gccgtttaat ctataggctc cgttttgata acatttcagc actaccaacg gatccgacat 15120gtaaacttga cgcgttagca cgtccaattc agcgtaatgt tggtcgacgc atttttgtaa 15180attagtttgc aggttgcaaa acatttttgc gcaaaagccg taatagtcaa aatctatgca 15240ttttaatgcg cttctgtcgt cgtcaatatg gcatgtcacg gctgcgcctc cagttaacac 15300gaataaaccg ccgttttcgc aaactacggc ttcgaaacaa tctttgataa atgccaactt 15360tgctttagcc acaattttat cgcgcaggcg atcttcaata tcctttgtcg taatataagg 15420taggacgcca agatttagtt gattcaacaa acgttccata atgaatagcg gcgacgcaac 15480acgactacac tgttcaaatg cgcacgcaaa acaaaccctt gcaactttat ttgccaatcg 15540taatcacagt agtttttacg agtacgccat cgcgtttgta agcacattgc tttttaaaaa 15600taatttaaat ttaatgaccg cgtgcaattt gatcaactcg ttgatcaact ttgaactcaa 15660catgtttggt aaaagtttat tgctaaatgg atttgttaat ttctgcattg ctaacagcga 15720cggggttacg attcaacata aaatgttaac caacgtgtta agttttttgt tggaaaaata 15780ttattaaaaa taaataaata aacttgttca gttctaatta ttgttttatt ttttataaaa 15840taatacaatt ttatttatac attaatactt tggtatttat taatacaatt atttacaata 15900ctttatttac actataatac tttatttaca ttagtactaa attaatacta aattacgcta 15960atactaaatt aatactttat ataatcaaaa ataatacttt atataatact ttctaatcat 16020cataaacggg taatagtttt ttctcttgaa atttacgctg caactcttcg ctaaaacaca 16080tgggcggtgg agtgggagcg ggtggagtag gagtccttac gggtttgatg ggcgacagtt 16140ctctggactt gcggaacagc ttgggcgaaa acgtcggcgt gcgccgacta atgatttctt 16200catcgcacga ggcgtcgcac attgtgcacg cgtccggtga ggtacacaaa actttcttgg 16260gcacgctgta caccggcttg ggcacgctat atgtgttgcc aaaactagaa ctcgttgtgg 16320ttgccgaacg gagacgatgg gtgtgaagac ggcgatggct gtgaagacaa gtccgaaggc 16380gcgataaaag atgaaagtgt ttctgaaacc gaagtggtgg tagaagtggt agaaggcggg 16440tgcgttacgg caaccacgct gctgctattt ctgccttcgg agaccacttc cagcaatcta 16500gagttactct ctcgttcttc gcggcgatag tcaatgtcgc aataatgttc ataagatgcc 16560ttttcggctt cggcgcgcct tttcatgtat atgttgtgac gcatctcctt taactgcacg 16620tacaaattcc agcattgcac agccagtatc gtaagcacgc ccattatgat tacgggataa 16680ttttgattaa acacggtcgg ctcgtgatcg cttacaatcg ctcggcacat gatgcatttt 16740ttgtaaatgt tcacatacac acagttttgg ctcaaggttt cggtatttgc gtagtcaatt 16800tccagataca cgatagagtt ccagcacatt gattccaaat cgtagtgacg atataaaaca 16860tctagcgccg gtagatgacc atttttgaac acgtagattt gaaacgcggc aaacagcatc 16920caacacagcc cagtgatcac gtttaccata atacacgtga tagcgacgta aaagttttct 16980ttcgcattga aatttacatt tgtgtttgaa gagctgctgc gatttttcgt ccacacgata 17040atcttccata taaaataaaa catgtaaaat aatatccaca tgccgaacgc cagcattatc 17100ggtatagata gattgataac cgattgcttt ccttcaattt ccagcaaaaa cgcgtatctg 17160ctgtctatca ctcccattat agataacaca aacactatca gatatgctaa taataatgag 17220gcattaagcc cgaattgtaa aactgcagtg attttattta acattttgaa tatttaattc 17280aacaactaag taatggcaat atgtatcgag tactgatcgt gtttttcctg ttcgtgtttc 17340tttatatagt gtaccagccc ttttatcagg catacttgca tatcggacat gcccaacaag 17400attacaatga cacgttggac gataggatgg attacattga atccgtaatg cgtagaaggc 17460actacgtgcc gattgaagcg ttgcccgcaa tcaggtttga tactaatctc ggcacgttgg 17520ccggtgacac gattaaatgc atgtcggtgc ctttgtttgt tagtgacatt gacctgccga 17580tgtttgattg tagtcagata tgcgataacc cgtctgcggc gtatttcttt gtcaacgaaa 17640cggatgtgtt tgtggtcaac ggccacagac tgacggtggg cggatactgc tccactaata 17700gtttgccccg caactgtaat cgcgagacga gcgtcatttt aatgagtctc aatcagtgga 17760cgtgcatagc cgaggacccg cgttactatg cgggcacaga taacatgacg caactcgcag 17820gcagacaaca ctttgaccgc attatgcccg gacagagtga taggaacgtc ctgtttgacc 17880gattactagg ccgagaggtg aacgtgacca ctaacacgtt tcgccgcagc tgggacgagt 17940tgctggagga cggcactagg cggttcgaaa tgcgctgcaa cgcccgagat aacaacaata 18000atctcatgtt tgttaatccg cttaatcccc tcgagtgtct cccgaacgtg tgcactaacg 18060ttagcaacgt gcacaccagt gttagacccg tatttgaaac gggagagtgt gactgcggcg 18120acgaagcggt cacgcgtgtt acgcacattg tgccggggga caggacctct atgtgtgcca 18180gcattataga tggcctggat aaaagtacgg catcatatag atatcgcgta gagtgcgtta 18240atctgtacac ctctattcta aattattcta ataacaaatt gttatgtccc agtgacactt 18300ttgatagtaa cacggacgca gcttttgcct ttgaagtgcc cggctcctac cctttatcgc 18360gcaacggcat caacgagcca acttatcgct tttatcttga taccagatct cgagttaatt 18420acaatgacgt cagagggcag ttatcttaat tgtgataaca caaacaataa gtcatttaaa 18480tgttacgtca gtagttagta tataagccgt acatgttggc ttgcaaattc agtcaatatc 18540aggcttttat catggacggt gtaaagctgc tagggacgtg cgcgctaata attttgttat 18600cgacgacgag tacagttgtc gggcgtgacc gtatcacgtt tacgccgata gaagatagcg 18660caggcctcat gtttgaacgc atgtacggct tgcgacatca tacagacgac agatttgtgt 18720ttgtgaaaaa attcaatttt gtttcggtgc tgcaagagct caataatatc aaatctaaaa 18780ttgaattata tgaagcgcaa gtttcaactt gcacaaacgt cagacaaata aaacagaaca 18840gatcgagtat catcaaagct cgcattgaaa atcagctgca gtttttgacg caactaaaca 18900aaaatctcat cacatactct gtggaaagca gcattttaag caacgacgtg ctggacaaca 18960tcgatctgga atatgacgac agcggtgagt ttgacgttta cgacgaatac gaacagcctt 19020cgcattggag caacatgact gtatccgacg cgcaagcttt gctccgaaac ccgcccaaag 19080acagagtaat gtttttggac acggttacca ccagcgacgt gagcagcaaa tacgaagaat 19140acataaactg cattgtgagc aaccgtaccg ttgaaaacga gtgcatgttt ttagccaaca 19200tgatgaacgt gctcaacgac aaattggacg acgcagcagc tttggccaag atgctggagc 19260gaatagtaaa acaaacgcga aagaacaaac tcaacatctc caacacggtt atagacgacg 19320acacgctgct aacggaaatg aaaaaattaa cacaaacttt atacaaccaa aaccgcgtgt 19380gggtagtgga ttttaacaag gacatgaata gttatttcga tttgtcgcaa gcgtataaat 19440tgcatttata tgttgattta aacacggtca ttatgtttat taccatgcca ttgttaaaat 19500ccaccgccgt ttcgtttaat ttgtatcgcg tcatgacggt gcctttttgc aggggcaaaa 19560tgtgtctgct tatcatttcg ggcaatgaat actttgggat tacagacagc aaaaactatt 19620atgtgcccgt atctgataac tttagacaag attgccaaga gtttacgggc tacaatgagt 19680ttttgtgtcc cgaaactgag ccgattgcca ctatgaactc gaaagtgtgc gagattgaaa 19740tgtttatggg tcgatatagc gacgacgtgg acaacatgtg cgacattagg gtggccaatt 19800ataatcccaa aaaagcttac gtgaacactt taatagacta ccgaaaatgg ttgtacattt 19860ttccaaacac gaccgtgtcc gtccactatt attgtcacga cgcgcttgta gaagttgata 19920caaaagtttc gcccggcgtt ggtgttatgt tttcgactat ggcgcaaacg tgttcgatta 19980gaataacgta tgatgtgacc ataactgtag attcgcgatt ttatgtcagc cattcaacta 20040catactggcc taaaaagaaa tttaatttta acaactacat cgaccaaatg ttgcttgaaa 20100aagcgaccac cagttttata ccgactgttg acaattttac ccggcccgtt ttattgcaac 20160ttcctcataa atttcacatt aaagattaca catcgacgcc ccatcatttt ttccatcagt 20220ctaaaattta caccaacagc gcggcgcccg acgaagactc gcaagacgac agtaatacca 20280ccgtggttat tatcgctatt gtcgctgcaa tgatcctatt ctgtggatta ttgttatttt 20340tgttttgctg tataaaaaaa cggtgtcatc aatcaaataa cgtggttgtg caatacaaaa 20400ataacaatga atttgtcaca atttgcaata atttagaaga caatcgagca tacattaatt 20460tacctaatga atacgatagc gatgatatgc caaaaccatt gtacccttta cttggcttta 20520atgatgattt gttaaaagat gataaacctg tgttgtaccc tatgattata gaaagaataa 20580aataaaacat gtataattga aataaatata ttatttaata aaatgttttt tatttatata 20640ctattttcta ttacatattc caatgcacac aaatgtttaa tggctatcag ttttaatttt 20700actaattcgt ctaaacaaaa attattcact tgctgttttt catccatttg acatatggcg 20760tttataaata attcgctgtg ttttatgaac gaatcgtaaa ccgctgcctg ggccttcagc 20820acggtcggcg cattgtattt ttgggtaaag tacgcaatat ttttagtcaa acacagagat 20880tttaaatctt tttcatttat atccaagtcg gaacaatcgt atacaaaatc tagcttttca 20940ctttcgggcg cgcccagata ctggtttacg agttcgagct gctccacttg gcctttgata 21000tcggccgcta tgcacaacat tttgtcgatt gcagtttcat tgtttttaac ataataattt 21060ttaacttttt tattttgcaa tttaatcaaa ctatttaaat tcgcttgacc tttcttacaa 21120agcgcagtta atatgcaaga cattttgact tataataaaa aacaaaactt ttatatattc 21180atttattgtt caataataac aaatattcca ggcttaaaag ctaacgaata gggcttttcg 21240gtaattttct tattattcat gtccgtcatc tgcatctctt tgccgtactt gacgccgtca 21300atggtgccca tcatgtacat tttaatctcc tccgaaggtc cgtctatttt gtccatttcg 21360aacaatctat caaaatcttc aacgctcatt ctctgcatat caagaggaac gtttctgatc 21420tttccggtgg cgtaaattga tccgttgttg tcacggttga ttatgtaaaa ccgacgaatc 21480aacatgtcgc gctcgctagt tttgttctta tccggcaaat gaatgcacac gtttggttcc 21540atcttcaaag gaaaatcgct ttgcaagtgt ttttgcaaaa tgttgccaaa tatattgttg 21600tgtttgtgaa tgtctccgta ttgaatgcta aaaaactggc caaagttgct tttggcacgt 21660tttatggttc caaagtcgga aaaccaaaat ccgcagggct tgccctgcac tcttggaccg 21720atggtgtacg tagtcttgcc gttggccggc tccaacacca cgatattttt atcgggctcg 21780ggatacaact tgtcttccca ttcgtgcaaa ctgttcaaat tagacagtcg acaaaattcg 21840tttttcaaaa atctgccttc gaaacaacta caattcagta ttgaaaagtt gcctcgtttc 21900acattaatcg ccatctgctc ctgccacaac atcttcgtca actcgtgtgg ctccaattga 21960atggacgacg gcgtaaaata gcacattacg cccgtttcgt cgtgtttcac gttaaaagcg 22020ccgctgttgt acggcaccag ctgctggtcc tcaccacctt ccgatctttc ccgcttcggc 22080tggttgtcgt cgctgctcga atatccatcg ccaatcttgc gtttagttgc catgctaccg 22140acgtgcgctg tctgctgtgg ttcaagtcta attgaagtgt ttcacagaat ataagatata 22200taataaatat ggacgactct gttgccagca tgtgcgtaga caacgcgttt gcgtacacta 22260ctgacgattt attgaaaaat attcctttta gtcattccaa atgcgcccct ttcaagctac 22320aaaattacac cgttttgaag cggttgagca acgggtttat cgacaagtat gtggacgtgt 22380gctctatcag cgagttgcaa aagtttaatt ttaagataga tcggctaacc aactacatat 22440caaacatttt cgagtacgag tttgtagttt tagaacacga tttgtccaca gtgcacgtca 22500ttaacgccga aacaaaaacc aaactgggcc atataaacgt gtcgctaaac caaaacgacg 22560caaacgtgct cattttgacc gtaactttaa cgagctaaaa tgaacgagga cacgcccccg 22620ttttatttta tcagcgtgtg tgacaacttt cgcgacaaca ccgccgaaca cgtattcgac 22680atgttaatag aaagacatag ttcgtttgaa aattatccca ttgaaaacac ggcgtttatt 22740aacagcttga tcgttaacgg gtttaaatac aatcaagttg acgatcacgt tgtgtgcgag 22800tattgcgaag cagaaataaa aaattggtcc gaagacgagt gtattgaata tgcacacgta 22860accttgtcgc cgtattgcgc gtatgctaac aagatcgccg agcgtgaatc gtttggcgac 22920aacattacca tcaacgctgt actagtgaaa gaaggcaaac ccaagtgtgt gtacagatgc 22980atgtccaatt tacagtcgcg tatggatacg tttgttaact tttggcctgc cgcattgcgt 23040gacatgatta caaacattgc ggaagcggga cttttttaca cgggtcgcgg agacgaaact 23100gtgtgtttct tttgcgactg ttgcgtacgt gattggcata ctaatgaaga cacctggcag 23160cgacacgccg ccgaaaaccc gcaatgttat tttgtattgt cggtgaaagg taaagaattt 23220tgtcaaaact caattactgt cactcacgtt gataaacgtg acgacgacaa tttaaacgaa 23280aacgccgacg acattgagga aaaatatgaa tgcaaagtct gtctcgaacg ccaacgcgac 23340gccgtgctta tgccgtgtcg gcatttttgc gtttgcgttc agtgttattt tggattagat 23400caaaagtgtc cgacgtgtcg tcaggacgtc accgatttta taaaaatatt tgtggtgtaa 23460taaaatggtg ttcaacgtgt actacaacgg ctattatgtg gaaaaaaaat tctccaagga 23520gtttttaatt catattgcgc ctgatttgaa aaacagcgtc gactggaacg gcagcacgcg 23580caaacagctg cgcgttctag acaagcgcgc ctacaggcag gtgttgcact gcaacggcag 23640atactactgg cccgatggca caaagtttgt ctctcatccg tacaacaaat ctattcgcac 23700gcacagcgca acagtcaaac ggaccgacag ctcgcatcga ttaaaaagcc acgtggtcga 23760caaacgaccg cgccgctctt tagattctcc tcgcttggac ggatatgttt tggcatcgtc 23820gcccatacca cacagcgact ggaatgaaga actaaagctg tacgcccaga gccacggcta 23880cgacgactac gacgacaatt tagaagatgg cgaaatcgac gaacgtgact ctttaaaaag 23940tttaaataat catctagacg acttgaatgt attagaaaaa caataaaaca tgtattaaaa 24000ataataataa taaaactata ttttgtaata tataatgtat tttatttaaa aattgtctat 24060tccgtagttg agaaagtttt gtcttgactt cataactctc ttctccatat tctgcagctc 24120gtttacgttt tttgtgacgc ttttaatttt ctcaaaatgc tggctgtcaa tagttatttt 24180ttgcttttgt ctattaattt cttccaattg agattttaaa tctcgctgag attgagatgc 24240gttgtaattc cttgagaaca tcttgagaaa acatacagat gaggtaaaac agcatctttt 24300atccaaatta ggagttaatt attattcatt tgtatcgcga ccatttgctc gtacacatct 24360tccataaaat ggttattttt attgcgataa gtgttggcat tgacattttg caaatgtcgt 24420aggttaaagg ggcaaatggg ctgcgtggcc gataaaagat tccagttcaa caatccctct 24480tcgcccccgt ttaacttgaa aatggcgcta cacgtttcta cgctatcgtg ttcctgttga 24540gtggcgcacg gttcgaccag tatcatcttg tgatatgcgg ttttgacatt catgtgcaac 24600ggaataactt gcgggtcatc gcattcgtcg gaattaagct ttaaatggcg tccgtatgct 24660ttccaaagtt tttcgtcgtc gaaccgcggc actgcttgca agtcgacgcg gggaaacggc 24720gctctgtaca aaacgcctaa attcaaaaac tgattgcatt gttgcagctc tgtccaatcg 24780acgcgatttt tgtaattttg aaacagcatc aggttgaacg ccgcgctggc gcgcacgttt 24840gtaatcactg tgtaattgat cagcttgtgc caatactggg cattgaaatt ttcttcaaac 24900tcatttctaa actctggatg cgcaaacatg tgtctaatgt agtacgcggg cggggcgttg 24960aacgcagtcc atttgtcaat acacttccag tctgaatgta acgtgttcac caaaccggga 25020tattcgtcaa acacgagcat gtgatccgac cacggtatgc tgtgggcgat caattttagt 25080tcttgcacgc ggccttcgcg taagcaatac aaaatgagcg cgtcgctgat cttgacacag 25140tcttgcatgt acgcggacaa attaacgttt tccatacagc tcacattgtt tattagcgcc 25200gtgttcaagt gtttgtattt ggacacataa tcgtagttga tgtactgttt aatgggttct 25260tgaaaccatt cttttagtag tatgtgactg gccactatgc gtttccaatt taatttgtgt 25320gcgtattttt gctgcaccga caacgagagg ttattgtaat ttttggatat ttcttccatg 25380tccaacaagt ccccaaacgc gagtataaaa tcttgcgtca aaaatttttg ctcagacacc 25440aacgaccaga tcaaatgtga tttaaacctg ttggcgattg ttatcgacaa cggcgaaatt 25500gaaataattt tccaatccaa cttgttgcga aacacgtgaa taaaatcgac gcgtccgtaa 25560cattcgcgcg atatgcgctt ccaaaacgtg tcatcttgca aattaagcaa atagacacga 25620ttgttgggag atttgacggc caattcaatt atttttatat attctttttg ctttaaagcg 25680cgttgtagca cttgggttgg agccatgtcg actgaagctc cacgctgttt gaagcaaggt 25740gaccgttttg gtcggcatgt tcaaacgtcg attacatgtt tgctttgcat caaaatggcg 25800taattaatta agaaacaaca tgaaagccat ctgcatcatt agcggcgatg ttcatggaaa 25860aatttatttt caacaagaat cagcgaatca accgcttaaa attagcggct atttgttaaa 25920tttgcctcga ggtttgcacg gctttcacgt gcacgaatat ggcgacacga gcaacggttg 25980cacgtcggcc ggtgagcact ttaatcccac caatgaggac cacggcgctc ccgatgctga 26040aattaggcat gttggcgact tgggcaacat aaaatcggct ggctacaatt cactgaccga 26100agtaaacatg atggacaacg ttatgtctct atatggcccg cataatatta tcggaagaag 26160tttggtcgtg cacacggaca aagacgattt gggccttacc gatcatccgt tgagcaaaac 26220aaccggcaat tctggcggcc gtttgggatg cggaataatt gccatatgta aatgatgtca 26280tcgttctaac tcgctttacg agtagaattc tacgtgtaaa acataatcaa gagatgatgt 26340catttgtttt tcaaaactga actcaagaaa tgatgtcatt tgtttttcaa aactgaactg 26400gctttacgag tagaattcta cttgtaacgc atgatcaagg gatgatgtca tttgtttttc 26460aaaaccgaac tcgctttacg agtagaattc tacttgtaaa acataatcga aagatgatgt 26520catttgtttt ttaaaattga actggcttta cgagtagaat tctacttgta aaacacaatc 26580gagagatgat gtcatatttt gcacacggct ctaattaaac tcgctttacg agtaaaattc 26640tacttgtaac gcatgatcaa gggatgatgt attggatgag tcatttgttt ttcaaaacta 26700aactcgcttt acgagtagaa ttctacttgt aacgcacgcc caagggatga tgtcatttat 26760ttgtgcaaag ctgatgtcat cttttgcaca cgattataaa cacaatcaaa taatgactca 26820tttgtttttc aaaactgaac tcgctttacg agtagaattc tacttgtaaa acacaatcaa 26880gcgatgatgt cattttaaaa atgatgtcat ttgtttttca aaactaaact cgctttacga 26940gtagaattct acgtgtaaaa cacaatcaag ggatgatgtc atttactaaa ataaaataat 27000tatttaaata aaaatgtttt tattgtaaaa tacacattga ttacacgtga catttacgat 27060ggcgaacaat aatttcactt tttatattag gacacgacgt gtatatagga aagcttaagc 27120gtttcaataa agccatggcg tacacgctaa gcttgcccag cttgcggctc tttgaaatct 27180gtagttttcg gggagtaccg tcgttcttca gtgccacata cgtcaacttg cgatcgtaca 27240ctttataata cgtgttgtag ttattttttt ccagaaattc cctcataaag caatccttgg 27300ataaagtttt tgatccgtac agttggccac accggtccat gcacaggtac acacacgtga 27360tggcgttttg aatgacgatg cgatttctgt caacggcaac gcgcttgaat atggtgtcga 27420cgttgtccga ttcaatggtt ccgtaaacag ctccgtctgg atttactgcc aaaaactgcc 27480ggttaataaa cagctggccg ggaatagacg tgcccgtgat gtgtgtcagc agagctgagc 27540agtcagccat agaggctaga gctacaagtg ccagcaagcg atacatgatg aactttaagt 27600ccccacagca aactggcgct tttatataaa aatttgggcc atttttggcg attagataat 27660ttttgaagat tagataatat tgagattagt taataatttg tgtgattaga taacttttta 27720gggtattgcg cattataaat caaggtcgag ttgtataaac tgctctggcg tgtaaaactg 27780cagacttaag ttttttgcaa acactcggtc tgaatcgcta aaatctttct gaccggtggt 27840tagattaatt cggccagccg cgtcgcccac ataaaaagat tgttccttgt caatatgcgt 27900aaactgtttg gccatctcgc gccacattcc cgtgtcgggc tttcgatgct catccttgtt 27960gggcgacaca taaaacgata tgggcacgcc agtagctttt ttaatattct ctaatttata 28020taataaatcg ctcgctttga ttttgccgga acctaaatgg gcttggttcg taaaaacaac 28080taaatcgtag cctaattcgt acaaacgctt tagcttgtgt gcgcacggaa ggagctgcca 28140gtcgtctggg ttttttggaa atttggaccg tgtctttgag ctaattagcg tgccgtccaa 28200atcaaaagcc gcaattttgg ttcttttagc gccgtcatga accgcgtacg catacaaatc 28260gggctgctgt aacgtccaca tggtgaatgc atcttactca aagtccatca attcgtacgc 28320gtttgtgtcc aggtcgggcg ttgaaaaatt gtagcttgcc attagatcgg atagcgattc 28380aaattttgta agcgtttgta gcgcacgttt ggcatcttgt ttaaaattac acgacgacag 28440acagtaaaaa tattcctcga taagcatgac tacacccata tcactgttta agtgctcgac 28500gtagttgttg catgttatgt cgcgtgtgcc gcgatacgcg tgatttcggt gaaaatcaca 28560ccacaaccag tcggcgtgcg tgtaacaaag tcgacagcga aacaatttat cgttttccaa 28620aaaatttaaa tactcgacag ttttgcagct tagattccgc gtttgattca ccttaaaatc 28680gtcgtcagcc tctataatct cgggcaacag cttgccttgt tgccccatcg tatcgatcac 28740ctcccccaag tggcccggtg ttatattaag tcgtttaaaa tcatttattg cttcctgcac 28800gtcggcctgg taatttttga ccacgggcgt ggaaatcaat tgccgttgaa gggaaataat 28860tcgtggtgtg ggtatcggcc gcctgttgca caattccacc agcggtggag gcaagggcgc 28920attcacagca accgttgtca tttataagta atagtgtaaa aatgcaaata ttcatcaaaa 28980cattgacggg caaaaccatt accgccgaaa cggaacccgc agagacggtg gccgatctta 29040agcaaaaaat tgccgataaa gaaggtgtgc ccgtagatca acaaagactt atctttgcgg 29100gcaaacaact ggaagattcc aaaactatgg ccgattacaa tattcagaag gaatctactc 29160ttcacatggt gttacgatta cgaggagggt attaataata acaataataa aaaccattaa 29220atatacataa aagtttttta tttaatctga catatttgta tcttgtgtat tatcgctaac 29280cattaaaagt gctggagcca cagtgttgcg gcgagtcttt atagaagatc gttgtttggc 29340tggaactgag cttttccttt tcctgctgcc gctaatggga gtgggcacgt actctgtagt 29400agacggtgca acgggcaact tgagcgctac cgtcttaaat ttggccatac ttttagtgat 29460gaaatcgcgc gttaacactt cgtcgtaaat gttacttagc agaggcgcaa cattgtgatt 29520aaatgtctcg tttaacaagc tgtaaaactc cgaataaagc ttatcgcgca tttcgcagct 29580ctccttcaat tctgccaaat ttgcgttggt aagcaccaca gtctgtcttt ttttgctcgc 29640tggaattgct gcgttctcgc ttgaagacga cgatgtcgat cggtcggcca tttttttgcc 29700cagcttttca gtgtgatcaa aaatgaacac aaaatctgcc aattcgggct tgtttttcac 29760caaatcccac atggccgggc tactaggcca ctcgggctgc ttgatcttag tgtaccaact 29820gttaaacaaa atgtatttat tgttgttaat cactttcttc ttgcgtttgg acattttgcg 29880ttcgtcttgc atgacaggca ccacgttaag gatatagtta atgttctttc tttccaagaa 29940atttacaata acggccagct ggtccatgtt ggatttgttg taagagctcg attccagttt 30000attcaacagc ttttcatttt tgcacacggc cgcagtctcc ggagattgtt gctccggcac 30060gtttaccatg

tttgcttctt gtaaaccttt gaaacaaccc gtttgtattc ttgatgatat 30120atttttttaa tgcccaacaa cctggcaatt cgtttgtgat gaagacacac cttacgcttc 30180gaacatttgt cggtgattac tgtgaaatgg cctaaattag ctcttatata ttcttttata 30240cgctcaaacg acacgatgtc caacatgtgc gcgcagacgt tttctgtgtt catcgtgtgc 30300ttgagcgtgt tgatggcttc cctgaacagc gcttgtattt cgctgcgagt caagcagtcc 30360gaatcacacc cgcctaagtg cgtgcaattt ttggggggca tcgttgtcta tctttttcag 30420agtggcgtag aaaaagtcct gcaattgcct attatcaaaa cgcgccttga cgctgcgcac 30480aaaatcaaaa aattcaatgt aattgctgta atcgtacgtg atcagttgtt tgtcgttcat 30540ataattaaag tatttgttga gcggcacgat ggccaggctg cgcgctattt cgcaattgaa 30600gcgtcgcggt tttaacatta tacggtagtc attgccaaac gtgcccggca acaacttcac 30660ggtgtacgtg ttgggtttgg cgttcacgtt aatcaagttg ccgcgcacga cgcctacgta 30720tatcaaatac ttgtaggtga cgccgtcatc tttccattgt aacgtaaatg gcaacttgta 30780gatgaacgcg ctgtcaaaaa accggccagt ttcttccaca aactcgcgca cggctgtctc 30840gtaaactttt gcgtcgcaac aatcgcgatg acctcgtggt atggaaattt tttctaaaaa 30900agtgtcgttc atgtcggcgg cgggcgcgtt cgcgctccgg tacgcgcgac gggcacacag 30960caggacagcc ttgtccggct cgattatcat aaacaatcct gcagcgtttc gcattttaca 31020tatttgacac ttaaaaaatt gcgcacacga gcaccatcgt ttgataccta attgcaacta 31080tttacaattt atcagtttac gttgaacccg ttttaatttt ttagatccgt ccttgttcag 31140ttgcaagttg actaaatgac aaaatttttc ggttctgcaa aaccgccctt gtctgttcca 31200cccgttgtat ttgaaaaaac tttttttcac gcggcgacaa ctgcttgtat aatattgccc 31260aatgtaaaca tgcaaaattt tgttactctc gtcaaaacag cggttggcgt tccattccat 31320aattttttta ttatttatca acgatggcca ttgtaaattg tcgtcattta tacgcatcat 31380atgatttaac aaaagctttt cgtatagcgg aacttcaatt cccttggaac atttttcaaa 31440cgataattta atttgtttct cggttggcag catttcatgc ttgattaaca atcgcctgac 31500ttttatagcc acgtttatgt ctttgcacag caaatgtggg ttgtcgacaa tgtaatagtg 31560caaagcattt gttacggcaa atgcgtagtt tgatttgacg acgccctttt tcttgacggg 31620cattgcggct tttaaaatta cttgcaagca ttgtacgaat acctctttgt gtttaaacaa 31680taatatggac aaacatcggc gaaacaattt gtaataatta tgaaatccca aattgcaggt 31740tttaaacttc tttgttactt gttttataat aaataaaatt tgctgaccca tgtctgcgcc 31800cacaacttta attaaccatt tgtgcgcata ttgattgtct cgttgttccc aaccggaaaa 31860ttgattgatc tcgagccacc ggcattggtc gtttgatacc gtcgttaacg ccgacgctcc 31920tgcctgtttg attacgggtt ctaaaagacg aaacagcagc gtaaatttgt ttttgcgtcg 31980gtagtatttt ggcaggcaat aatcaaaaaa atccgtaagc aattctctgc atctattaat 32040attcgttgcg tacgaatcga gtttttcaaa aattactttg tttgtatgaa aataacgttt 32100gggcttctca caataataat cttcgttgta gaacagaaac ggtttgcgag aattggcacg 32160tttgtccatg attggctcag tgtaacgatt gattcaaatc aaaattgaca acacgtttgc 32220cgtaatgtgc accggttcgc acacgtttgc cgcgtatgta atccatgttt atttcgctgt 32280cgcaattgat tacacgattg tgttgggcgg cgcgttttat tgaatttagg cgacgcgtcg 32340acaactccaa aggattgtaa agcgcagatt tttccagagt aaacgagttt aagtggccac 32400cgttgaacca ttccagagcc acgattgtgt acagcaaaaa gaatatttct ttgtcgacgt 32460tttcaaacgc aaacttgttt tttaggcaat agtagtaaaa ttttaacgaa ttgtataaat 32520aaaacataaa attgccattt ttaaagtaaa attctacatc cgtgacgaac aaaaggttta 32580ctattttgtt ctccaacaag tgtgccaatt ttcttaagta caccattgaa tttttgtcgt 32640cgtccatctc gatcaacaac acgtacggcg ttttggaatt taaaattatt ctaaaatttt 32700cctgttgcaa cgattccaca gcgtccgacc aatatgacgc tgccacctct agacagatgt 32760atttcttgga aaacacgtgt cgtttgataa cctcgctgat ggacgtgatc gattgtaaat 32820acttttcaaa cgtcgcgtct tcccaaccac gcaccgaaac gggcgctgtc gtgtcgggct 32880gatgtttgaa atccaaacca ctctgaatta acttggttgt gattcgtatg ctcaactgtt 32940gacccaacgt gtagtgatct tcgtaggcgc gctcccacat cacgttacac acaaatttga 33000cgagatcatc aacgtctttc tgttgcaaaa ttcgccgcaa acgcgccaca tcgcccttgt 33060accaccgatc tcggcacaca agctgtagca tttttaaatc gtgatcgctc aagctattaa 33120ttctggttag atttatatag tcgtcaatat cctcgggcgt ggtttgcgtc atgtctgtaa 33180aacgtgcaaa atcaaacatt tttatgttgt agtcgaatct aacaaatcca tcggcgttca 33240cttgcacttc gcgctttaca aaacgaggta gcgtgtaatc gaacccgttt aaatagattg 33300cgtacaaaac cagcacttca tcttccagtt tgcacgcttg cggcaaaaat tgtgtggtgt 33360gctccaaccg ggtgacaaac atgactatgg aaaataacgc ggaattcaac agacgactag 33420agtacgtggg cacgatcgcc acaatgatga aacgaacatt gaacgtttta cgacagcagg 33480gctattgcac gcaacaggat gcggattctt tgtgcgtgtc agacgacacg gcggcctggt 33540tatgcggccg tttgccgacc tgcaattttg tatcgttccg cgtgcacatc gaccagtttg 33600agcatccaaa tccggcgttg gaatatttta aatttgaaga aagtctggcg caacgccaac 33660acgtgggccc gcgttacacg tacatgaatt acacgctttt taaaaacgtc gtggccctca 33720aattggtcgt gtacacgcgc acgctacaag ctaacatgta cgcggacggg ttgccgtatt 33780ttgtgcaaaa tttttcagaa acaagctaca aacatgttcg tgtgtatgtt agaaaacttg 33840gtgcgataca agtagcgaca ttatcagttt acgaacaaat tattgaagat acaataaatg 33900aactcgtcgt caatcacgtt gattagataa tgtccgtgtt aaatgtgata tcttagatta 33960cgagcgcgca ataaccatag tttaatcgaa gagaatagcc gtcgccacaa tggataatta 34020caaattgcaa ttgcaagaat tttttgacca agcgcccgac aacgacgatc ccaactttga 34080acatcaaacg cccaatctat tggcgcatca gaaaaaaggc atacagtgga tgattaacag 34140agaaaaaaac ggccggccca acggcggcgt gcttgccgac gacatgggac tcggcaaaac 34200gctctctgtg ctaatgttaa tcgcaaaaaa caactctcta caattgaaaa ctctaatagt 34260gtgtcctttg tctttaatca atcattgggt aaccgaaaac aagaagcatg atttaaattt 34320taacatttta aagtattaca aatctttgga tgccgacacg gttgagcatt accacattgt 34380ggtgaccacg tacgacgttt tattggcaca tttcaaattg atcaaacaaa ataaacagtc 34440aagtctgttt tcaacccgct ggcatcgagt tgttctagat gaagcgcata ttatcaaaaa 34500ctgcaagacg ggcgtgcaca acgccgcgtg cgctttgacc gcaacaaacc gatggtgcat 34560taccggcaca ccgatccaca acaagcattg ggacatgtac tcgatgatta attttttgca 34620atgtcgtcct tttaacaatc caagagtgtg gaaaatgtta aataaaaaca acgactctac 34680aaatcgcata aaaagtatta ttaaaaaaat tgttttaaaa cgcgacaaat ctgaaatttc 34740ttctaacatt cctaaacaca cggttgagta tgtacatgtt aattttaatg aagaagaaaa 34800aacgttgtac gataaattaa agtgtgaatc ggaagaggcg tatgtgaagg ctgtggcagc 34860gcgtgaaaac gaaaacgcac taagccgatt gcagcaaatg cagcacgtgt tatggctaat 34920actgaaattg aggcaaatct gctgccaccc gtatttggcc atgcacggta aaaatatttt 34980ggaaacaaac gactgtttta aaatggatta tatgagcagc aagtgcaaac gagtgctcga 35040cttggtagac gacattttga acacaagcaa cgacaagata atattggttt cgcaatgggt 35100ggaatattta aaaatatttg aaaacttttt taaacaaaaa aacattgcta cgttaatgta 35160cacgggccaa ttaaaagtgg aagacaggat tttggccgag acgacattca atgatgctgc 35220caatactcaa catcgaattt tgctgctttc cattaagtgc ggcggcgtcg ggttaaactt 35280aataggcgga aaccacattg taatgttgga gcctcattgg aacccgcaaa ttgaattgca 35340ggcgcaagac cgaatcagtc gtatgggaca aacaaaaaac acgtacgtgt acaagatgct 35400aaatgtggaa gacaacagca tcgaaaaata cattaaacaa cgccaagaca aaaagattgc 35460gtttgtcaac acggtctttg aagagactct gctcaattac gaagacatta aaaaattttt 35520caacttgtag ctggtaagtc gtcatgaaca cccgatatgc tacttgctat gtttgcgacg 35580agttggtgta cttgtttaag aaaacgttta gtaacatgtc cccttcggcc gctgcgtttt 35640accaacggcg catggccatt gttaaaaacg gtatcgtgct gtgcccacgt tgttcgtcgg 35700aactaaaaat tggcaacggc gtttcgattc caatttaccc ccaccgcgct caacaacatg 35760cacgacggtc gcgttaagac gcaagcgctt cgagttttgg cccgctcgct acctccgctg 35820tacgactcga ccgtcgatcg acacggctgc aaggtgttca cggtgcggcg ctacaacaga 35880cgcgtaatcg actttgcggg cattcgcaac aaaacgctgg aaatcattaa aacggataga 35940aacttgccgc tcaacacaga atgcaatgtg aaagttgtcg acagtgcatg catgcgttgc 36000agaaaaagtt tcgcagttta ccccgccgtt acctatctgc attgcggaca ttcgtgtctg 36060tgcaccgact gcgacgaaac ggtaaacgtg gacaacacgt gtcctaaatg taaaagcggc 36120attagatata aattaaaata caaaactttg taacatgttg ccctacgaaa tggtgattgc 36180cgtgttggtt tacttgtcgc cggcgcagat tctaaattta aaccttcctt ttgcatacca 36240aaaaagtgtg ctgtttgcca gcaactctgc aaaagttaac gaacgcatca ggcggcgagc 36300gcgtgacgac aacgacgacg acccctattt ttactacaaa cagttcataa agattaattt 36360tttaactaaa aaaataataa atgtttataa taaaactgaa aagtgtatta gagcgacgtt 36420tgatggtcgg tatgtggtta cacgcgacgt tttaatgtgc tttgtaaaca agagttatat 36480gaagcaattg ctgcgcgagg ttgacactcg cattacacta cagcaacttg ttaaaatgta 36540tagtccagaa tttggttttt atgtaaatag caaaattatg tttgtgttaa ctgaatcggt 36600gttggcgtct atttgtttaa aacactcgtt cggcaaatgc gagtggttgg acaaaaatat 36660aaaaactgtg tgtttacaat taagaaaaat ttgtattaat aataagcaac attcgacatg 36720tctatcgtat tgattattgt catagttgta atatttttaa tatgtttttt gtacctatca 36780aatagcaata ataaaaatga tgccaataaa aacaatgctt ttattgatct caatcccttg 36840ccgctcaatg ctacaaccgc tactactacc actgccgttg ctaccaccac taccaacaac 36900aacaacagca tagtggcctt tcggcaaaac aacattcaag aactacaaaa ctttgaacga 36960tggttcaaaa ataatctctc atattcgttt agccaaaaag ctgaaaaggt ggtaaatccc 37020aatagaaatt ggaacgacaa cacggtattt gacaatttga gtccgtggac aagcgttccg 37080gactttggta ccgtgtgcca cacgctcata gggtattgcg tacgctacaa caacaccagc 37140gacacgttat accagaaccc tgaattggct tacaatctca ttaacgggct gcgcatcatt 37200tgcagcaaac tgcccgatcc gccgccgcac caacaagcgc cctggggccc ggtcgccgat 37260tggtaccatt tcacaatcac aatgcccgag gtgtttatga acattaccat tgtgctaaac 37320gaaacgcagc attacgacga agctgcgtcc ctcacgcgtt actggctcgg cttgtatctg 37380cccacggccg tcaactcgat gggctggcac cggacggcag gcaactcaat gcgcatgggt 37440gtgccctaca cgtacagtca aatcttgcgc ggatattcat tggcgcaaat taggcaagag 37500cagggaatac aagaaatcct aaacacgatc gcgtttccgt acgtgactca aggcaacggc 37560ttgcacgtcg attcgatata catcgatcac attgacgtgc gcgcttacgg ctatttgata 37620aattcatact ttacgtttgc ctattacacg tactattttg gagacgaggt aatcaacacg 37680gtgggtttga cgagagccat cgaaaacgtg ggcagtcccg agggagttgt ggtgccaggc 37740gtcatgtctc gaaacggcac gttgtactct aacgtgatag gcaactttat tacgtatccg 37800ttggccgtcc attcggccga ttactccaaa gtgttgacca aactttcaaa aacatattac 37860ggttcggttg tgggcgtaac gaataggttg gcttactacg aatccgatcc cacaaacaac 37920attcaagcgc ccctgtggac catggcgcgg cgcatttgga atcggcgcgg cagaattatc 37980aactataatg ccaacacggt gtcgtttgag tcgggtatta ttttgcaaag tttgaacgga 38040atcatgcgca tcccgtcggg caccacgtcc acgcagtcgt tcagaccgac cattggccaa 38100acggctatag ccaaaaccga cacggccggc gccattttgg tgtacgccaa gtttgcggaa 38160atgaacaatt tgcaatttaa atcgtgcacg ttgttctacg atcacggcat gttccagcta 38220tattacaaca ttggcgtgga accaaactcg ctcaacaaca caaacgggcg ggtgattgtg 38280ctaagcagag acacgtcggt caacaccaac gatttgtcat ttgaagcgca aagaattaac 38340aacaacaact cgtcggaagg caccacgttc aacggtgtgg tctgtcatcg cgttcctatc 38400acaaacatca acgtgccttc tctgaccgtt cgaagtccca attctagcgt cgaactagtc 38460gagcagataa ttagttttca aacaatgtac acggccacgg cttcggcctg ttacaaatta 38520aacgtcgaag gtcattcgga ttccctgaga gcttttagag ttaattccga cgaaaacatt 38580tatgtaaacg tgggcaacgg cgttaaagcc ctgtttaatt atccctgggt aatggtcaaa 38640gaaaataaca aagtgtcttt catgtcggct aacgaagaca ctactatacc atttagcgtt 38700ataatgaatt ccttcacctc tatcggcgaa ccagctttgc aatactctcc atcaaattgc 38760tttgtgtatg gaaacggttt caaattgaac aacagcacgt ttgatttaca atttattttt 38820gaaattgtgt aattatattt agggagaatg tgatattcaa aagactgact gttaacacaa 38880aagactgata ttgttgttgt tacaaaatag ataataaaac aaaaaataaa ttaaatatta 38940tttatttatt aaactgttta attttaatgc taacgcgtac aaatcacgct gttccgacgt 39000ggacatggaa ttgcgcagaa aagtcttgat agtgtcgatt tcttcgccgt catccacttc 39060catatatttg atttcttcct cgatttgcat ttccaagttt gcgtattctt gcaaataata 39120atctagtcgt tgggcgacct cgccaatttt aaataataca ttatccgaca ccaaatgcca 39180gcgagtgact gtgcgctcca tcatcctggc actttttaat gtgaatatta aaaggttgtt 39240gcatatatat cgttaaacgt ttatgtttac tttcacgtta gctcgtttca ttgatgtaaa 39300catttagttt tataacagcg tcggtaattt tattttttaa agtaaacaga ccaaaatcaa 39360aggtgtcttc gacaggtacg attattttcc cattgacact gttttcgtgc acagatataa 39420ttttatcacc gtttattatt ttgcccaaac acacgtactc gtttcttctc aagccaacta 39480tttctaaaca attcactttt ctattatcgt gtacgcaatt aaaagtaaac gaagcgctac 39540aattgtcgta ttctattaca attctgcggc atttataaaa tttattaatg ttgacgcaaa 39600ttccatgcag cgcatccatt tcgtactgca aatgcggcgc aattaaaaaa tttcctcgtc 39660gttgttaaca atcttgggcg ctaaaaagca cgccaacacg cccacgtctt taatgcaata 39720ttccaatttg aacggcagtt cctcggacat gtatattgtc acggtgggcg ccaaaggagc 39780ggctttagca aaatgacaca agtaatcgcc cgcaaaagtg tgcgttacgg tttgctttgc 39840tttgagaacg gaaaagtttt cgttgtccgc gctcatctgc acgtccgccg agccaatgtc 39900gccatttgct ctaaactgca gacccttctt ggaacacgac acaataatat cgtggtcgaa 39960ttgcgtcatg tctttgcaca cctgcgcaaa ctcgacgctc gacatgtgga cgacgcaatc 40020gtaatcgcta tccggaattc ccaaatgttc cacgtcgatg cacatcaact tgagcgtgta 40080cgtgcagatt ctattgtcgt tgttgaacac gaacgccatc acatcgccct gatcttccgc 40140tttcatcagt acagagctgc gctcgttaac gcatttgaca attttactta aactgtttat 40200ggacacgttg agcggcacgt tgcggtcaca tctatatttt ttgaaaccct cggcgtgtag 40260ttgcaacgac acgagcgcga catgcgaggt gtccataacc tgcatgctta cgcctcgatt 40320atcacaatca aaagtagcgt gcggcagcag atccttaaaa gtttccacca gcctcttcaa 40380aactgcgccg gttttaaatt ccgcttcgaa catttttagc agtgattcta attgcagctg 40440ctctttgata caactaattt tacgacgacg atgcgagctt ttattcaacc gagcgtgcat 40500gtttgcaatc gtgcaagcgt tatcaatttt tcattatcgt attgttgcac atcaacaggc 40560tggacaccac gttgaactcg ccgcagtttt gcggcaagtt ggacccgccg cgcatccaat 40620gcaaactttc cgacattctg ttgcctacga acgattgatt ctttgtccat tgatcgaagc 40680gagtgccttc gactttttcg tgtccagtgt ggcttgtttt aataaattct ttgaaaatat 40740tgtcgggtgt attattaaat agcatgtatg gtatgttgaa gatgggataa cgcttggcgt 40800gcgggtcgtc atgatttcca ccgcgcacca catatttgcg ctcaatttta tcaaaattgg 40860actggcgaga caaaaacgag acgggcgaca ggcatatttg ggcgtgcgta ccatcttcgg 40920ccatccactc ggtcaggtct tcgctgcggt taaacacacc tttctgaccg tgaatgccac 40980atatttttat tccttccaaa tcgttggtgg acgtgactat gactatttta agcataacgt 41040tgtcgccgtt aaccaccatg ctggcgtcga gtttttcaat tttttgattt ttaatttgtc 41100taaagtaaac gtacactttg taaacgttaa aattgccgtt ggtgcacgtt tcaattttgt 41160accgtcggcc gtcgtacacc caattaatct ttgcgttgct caccaacaca ccggccatgt 41220acagcacaag tccgtcgtct agcgcaacgt aatttttgtc gctactattc gtaaacttta 41280ctaaacacga ctgcttgggg ccgaccacaa gcttgccctt caatttgttc actttgttgt 41340tgtataaaca aatgggcagc gcaatgtgcg gaatgtacgg atcttcggcg gtcatgagtt 41400tattgtctcg caccaacgtc cacaatttaa acattttatt gttgagcaaa atggacttgt 41460ttaccgccac agagtagcca tttggtaaac ccgatacgca attttcctct ttgtactcaa 41520acacgggcat ggcattcttt agattggtta gggacacaat caatttgggt acgggcgtgg 41580tatgaaataa atgtataaaa ttacgataat aatactgctc caacttggac atgagcgatt 41640tgacgtcatc gttttctacg atcgtacact gaataatggg attatagtat atagaatgtt 41700tatagtggta ttcgtagggt gtcaacaata cgttaatgtc ggcttcgttg ttcacccgca 41760actttttttt gatgcatatc attccttcgt gatgattaac gtaaagtatt ctgtctgtaa 41820tcttcaattc gatgggcgcc atgtttcttt tcatagtgta cacgataaac gacgtgtttg 41880attttaaaca ttttaaattt gtgggtctat cattaaacgc gatcagcaac gagtcgtctt 41940gaacgtcgtt gaggtcgtcc acgaacgcga ccagattgtg ttttagcaaa tattgaaatt 42000tttgcgcaac catttcgtag tccacgttgg gcaaacatgc gttgcggcaa aggaaaaact 42060ttttgcccgc cacggtcatt tcgccgtgaa aaaaactgcc aataaatttc acaaaatcct 42120ttttttgctt caacattttc tggcgcatgc tgtcgttggt gattcgcgcc acctcgttgc 42180cgacgcgata ttttaacacg ggcaacgaaa tttcaatatt gttattgctg ctgttgtcct 42240gttgattggg aaagactttg cgttgcttgc taaaagtttt cgatacgcaa tatatgagac 42300gcccgttgac tatacaatcg acaatctttt tcgactcttt gttgtacaag acgctttgaa 42360ttttacgacg cttgttcgcc accgtgtacg cgtcgtcgtc ggccgtcttg tcgagaactc 42420gttgatagtt ttgcaaaatt gtcgaagtta ataacagttc tatcaaatag gcgtgcttgt 42480atacaatttt gttggccaaa ctgtctatag aatagtttat gtcgtgattc ataataattt 42540ttatgtgttc cacgagttgt tgcttgtgaa gcgtgttgta ttcgaagaga aaatcgagcg 42600gtttccattt gccgctgttg gccagatatg tttccagcac agaatttaaa tcttccgtca 42660ctacgtaatc gctagcgtac acgtctcgag caaacaggac gtcgtcttgt ttgtcgtaaa 42720ctagttggat tgcgcgattg atgtgcttct cttgatccac gttgccgtac aaaaacatgc 42780gtttgcaatg tttggcgtat agcttgtcgt agaaattgtg caccaaaacg ttgttgttca 42840tcattatgtt gggaaaactc aaaaatctgc cgtccagcat aaaagttccg ttaatattgt 42900tgtttgcgtc gacatcgtcc gtttctctaa attgcttgtc taagcgcgtg ccgaatataa 42960cgggcacaca tttatgcatt acgcaactga gctgttcatt aagagcgcaa cacaaataag 43020acttgcgttc ttgaatagcg caaaaaagca tacgttcatt gctgtttgta gcgcaatcaa 43080aagtatattt taatttgtat ttattttcaa ttctatcgta caactcgttg aaatcttgaa 43140ccacgtccgt catcgtgaag cgattactgc gcactaatta tgtctaaacg tgttcgtgaa 43200cggtcggttg tttcggatga aacggccaaa cgcattcgac aaaacgaaca ctgtcatgcc 43260aaaaatgaat cttttttggg gttttgcaac ttggaagaaa ttgattatta tcaatgttta 43320aaaatgcaat acgttccgga ccaaaagttt gacaacgatt ttattttaac agtgtacaga 43380atggccaacg tggtgacgaa acaagttaga ccgtataaca gtatcgacga aaagcaccat 43440tacaacacgg tgcgtaacgt gttgatttta ataaaaaatg cgcgtttagt gcttagtaat 43500agtgtcaaaa agcaatacta tgacgatgtg ttaaaattga aaaaaaatac agacttggaa 43560tcgtacgatc cattgattac ggtcttttta caaattggcg aatctgtaaa tgaagaaata 43620caaaaactca gaaaagcttt ggtcaatatt tttactaata aacccgacaa gtcggatata 43680aacaacccag atgtagtttc gtatcaattt atttttggca gagtacaaaa attgtataac 43740agggcaatta aacaaaaaac taaaactata attgtaaaac gtcctacaac tatgaacaga 43800attcaaatag attggaaaac tctttccgaa gacgaacaaa aaatgactag acaagaaatt 43860gccgaaaaaa ttgtaaagcc ttgttttgag caatttggca ctatattaca catatacgta 43920tgtcctttaa aacacaaccg aattattgtc gagtatgcaa actcagagtc ggtacaaaaa 43980gccatgactg taaatgacga cactcgattt acagttacag agttttccgt ggttcagtac 44040tacaacgtgg ccaaaacaga aatggtgaac cagcgaattg acataataag caaggacatt 44100gaggatttaa gaaacgcttt aaaatcttac acataaatta aaatatcgaa caaaggaaaa 44160aaacaattgt aacaaaaata atttacatta aaatttacaa gtttttttct agtgtcgtac 44220ttttttacaa tgcgtctgtt gtccgtcgag cattgcaaac atattgtgga cggcgcaaaa 44280tagcaaacaa aaggcacgtc cgcgctctcc cacgctattc taaaacgatg aatccatatt 44340aatttttcat tgtcgccaaa cgtcgctccg ctgcctcctt ccaataacaa atactcagaa 44400acacaaacat gtacaattgc tgtcgcggcg ttaattgtcg ctgtttttcc aaatagtcta 44460ttatgggaaa caaacacttg tcacaacaca aatactcgtt aattgtcaca accgacaagc 44520acatttggca aaatgcgtcg caatttttgt acggacgaga ttctatgcga agttcgttgt 44580ccatgacgtc ttgggtccac tttttcaaca agacactttt atatttgtga tttgtacaac 44640tttggtacgt gttagagtgt ttttgataag ctttgataag tttaaaactg ttggagtaag 44700gccacgtcat tatgttctgc accttttgtt taaaagacag aaattactat atgttcaaac 44760tatttaaaga ttattggcca acgtgcacga cagaatgcca gatatgtctt gagaaaattg 44820acgataacgg gggcatagtg gcaatgcccg acactggcat gttaaacttg gaaaagatgt 44880ttcacgaaca atgtattcag cgttggcgtc gcgaacatac tcgagatccc tttaatcgtg 44940ttataaaata ttattttaac tttcccccaa aaacactaga ggagtgcaac gtgatgcttc 45000gagaaactaa agggtctata ggcgatcacg aaattgatcg cgtttacaaa cgcgtttatc 45060aacgcgttac acaggaagac gccctggaca ttgaactcga ttttaggcat ttttttaaaa 45120tgcaatcatg

acgaacgtat ggttcgcgac ggacgtcaac ctgatcaatt gtgtactgaa 45180agataattta tttttgatag ataataatta cattatttta aatgtgttcg accaagaaac 45240cgatcaagtt agacctctgt gcctcggtga aattaacgcc cttcaaaccg atgcggccgc 45300ccaagccgat gcaatgctgg atacatcctc gacgagcgaa ttgcaaagta acgcgtccac 45360gtaacaatta ttcagatccc gataacgaaa acgacatgtt gcacatgacc gtgttaaaca 45420gcgtgttttt gaacgagcac gcgaaattgt attatcggca cttgttgcgc aacgatcaag 45480ccgaggcgag aaaaacaatt ctcaacgccg acagcgtgta cgagtgcatg ttaattagac 45540caattcgtac ggaacatttt agaagcgtcg acgaggctgg cgaacacaac atgagcgttt 45600taaagatcat catcgatgcg gtcatcaagt acattggcaa actggccgac gacgagtaca 45660ttttgatagc ggaccgcatg tatgtcgatt taatctattc cgaatttagg gccattattt 45720tgcctcaaag cgcgtacatt atcaaaggag attacgcaga aagcgatagt gaaagcgggc 45780aaagtgtcga cgtttgtaat gaactcgaat atccttggaa attaattacg gcgaacaatt 45840gtattgtttc tacggacgag tcacgtcagt cgcaatacat ttatcgcact tttcttttgt 45900acaatacagt cttgaccgca attcttaaac aaaacaatcc attcgacgta attgccgaaa 45960atacttctat ttcaattata gtcaggaatt tgggcagctg tccaaacaat aaagatcggg 46020taaagtgctg cgatcttaat tacggcggcg tcccgccggg acatgtcatg tgcccgccgc 46080gtgagatcac caaaaaattt tttcattacg caaagtgggt tcgaaatccc aacaagtaca 46140aacgatacag cgagttaatc gcgcgccaat cagaaaccgg cggcggatct gcgagtttac 46200gcgaaaacgt aaacaaccag ctacacgctc gagatgtgtc tcaattacat ttattggatt 46260gggaaaactt tatgggtgaa ttcagcagtt attttggtct gcacgcacac aacgtgtagc 46320atcgccagta tttaacagct gacctatttg ttaaacaagc attcttatct caataattgg 46380tccgacgtgg tgacaattgt atccacaatc atgaaaaaag tagcgcttgg aaaaattatc 46440gaaaacacag tagaaagcaa atataaaagc aacagtgtgt cgtcgtcatt gtcaacgggc 46500gccagtgcaa aattgagttt aagcgaatat tacaaaactt ttgaagcaaa taaagtgggc 46560cagcacacta cgtacgacgt ggtcggcaag cgagattaca cgaaatttga caaattggtg 46620aaaaaatatt gacatgctgc gatcaatcat gcgacgtttc aagagtacaa acaatctcag 46680caaaaaaccc tccgattatt atgtagtgtt atgtccaaag tgttattttg tgacgtcggc 46740cgaagtgagc gtggctgaat acatagaaat gcataaaaat tttaacacga aattcgccga 46800tcggtgccct aacgatttta ttgtgaccaa ctctaaaagt tggaataatc atgaaaattg 46860ttctgcccta ttttaccctc tgtgttaata aagtttgttg tttgtatttt gtggttttat 46920ttatttacgc tagatattgg gtttaaggtt cttagaaata gagttgtatt ttccctacca 46980aaagggattt gagcttcata taaatacaat attcgctcga caagcggttt atttcactcg 47040gaggtattat atcaggcagt cgaacgtgcg cgatgaaaca tcccgtttac gctagatatt 47100tggagtttga tgatgtagtg ttagatttga ctagtttaat atttttagag tttgataacg 47160ctcaaaatga agagtacatt atttttatga atgtaaaaaa ggcgttttac aaaaactttc 47220acattacttg tgatctgtcg cttgaaacgc tgaccgtgtt ggtgtacgaa aaagctcgcc 47280taattgtgaa acaaatggag tttgagcagc cgccaaactt tgttaatttt atcagtttca 47340acgcgaccga caacgacaac tccatgataa tagacttgtg ttccgacgcg cgcataatcg 47400tggccaagaa gctgacgccc gacgaaacgt atcatcagcg cgtgtccgga tttttggatt 47460ttcaaaaacg taactgcata cctcggcccc caatcgagtc ggacccaaaa gtgcgagacg 47520ccttggatcg tgaactagaa ataaaactat acaagtagaa aaaaattaat ttattaatag 47580ttgtaataat tatcttcgtc ctcatcttcg ctggtgtcat aatgcggtgg tgtgtttgtg 47640ttttgtttta atcgtttgcg cgtcgacacc acttcgccga taggaaattt tttggatttc 47700gcattaaatg ccctcttagc gacgcgccgt ttacgactac taaacatgtt gacgcgctcg 47760tcgtcttcag tgtcataatc cgtgctagtg ttttcgttgt tattttctat gagacgatcg 47820tttgatttag ttttcgtaga attgtccgcg ttatcgtcgc tttcgtcgat gtcgtcccta 47880actatctcgt aggcggcttt gcgcggaatc caagattttg caatgtatct attttaacgt 47940acttttcttc gagcgctttt ctagctttat gcatagcaat gtcttcgtcg ccgccgttca 48000ttttatgata ctttgtaaac gtctcgacga ataacttttt ggcgcgagga ggcatttttt 48060cattgtataa catatcggga atttgataca ttgtaattag aattaagcaa gttcgtcttc 48120ggttgtactg tattcggttt ctgtatctgt agtggaatcc tctgtactag tagtagtgtc 48180gctattgttg gcgtcaggcc ttggctgcca tttaccgtct atcaacatgt attttttcct 48240aacagcacaa catgctagct tggtagctat ctgtgtcgac ttatattttt gtaaactacg 48300atcgtagaat ttttcaaata tcctcttacc gttataggga aggttttgat aatatttagg 48360caacatatca ataaaagaca atataaaaac tttgtgtttg tgttttattt atcacataaa 48420atggacgtct ggcaagaatc acaaccaata ttagtgtttt ttttcttaca ttacgagatt 48480caacttgata ctaaaattaa ttattaatta aattaaatta aattttgaag cattttttcg 48540ctatcgtttt cagactcaaa attatcgacg ctatcgctat gaaaagcgta atatttgttg 48600gctttgagat attctatatt ttgctcattt ttaacaataa acacgcgact cttttcgtcg 48660cgtctcacca taacaccgtt tttacaaatg gaaatgtatt tgtaaaacgg caacagagcg 48720tcgcgagttt ttttaagtaa cagcttttgc tccgctgtgg cggccacaaa tatttttacg 48780ggcccgtcgt aattaatgtt taaattaaaa tttttaagtc gacgctcgcg cgacttggtt 48840tgccattctt tagcgcgcgt cgcgtcacac agcttggcca caatgtggtt tttgtcaaac 48900gaagattcta tgacgtgttt aaagtttagg tcgagtaaag cgcaaatctt ttttaaataa 48960tagtttctaa tttttttatt attcagcctg ctgtcgtgaa taccgtatat ctcaacgctg 49020tctgtgagat tgtcgtattc tagccttttt agtttttcgc tcatcgactt gatattgtcc 49080gacacatttt cgtcgatttg cgttttgatc aacgacttga gcagagacac gttaatcaac 49140tgttcaaatt gatccatatt aactatatca acccgatgcg tatatggtgc gtaaaatata 49200ttttttaacc ctcttatact ttgcactctg cgttaatacg cgttcgtgta cagacgtaat 49260catgttttct tttttggata aaactcctac tgagtttgac ctcatattag accctcacaa 49320gttgcaaaac gtggcatttt ttaccaatga agaatttaaa gttattttaa aaaatttcat 49380cacagattta aagaagaacc aaaaattaaa ttatttcaac agtttaatcg accaattaat 49440caacgtgtac acagacgcgt cggtgaaaaa cacgcagccc gacgtgttgg ctaaaattat 49500caaatcaact tgtgttatag tcacagattt gccgtccaac gtgtttctca aaaagttgaa 49560gaccaacaag tttacagaca ctattaatta tttaattttg ccccacttta ttttgtggga 49620tcacaatttt gttatatttt taaacaaagc tttcaattct aaacatgaaa acgatctggt 49680tgacatttcg ggcgctctgc agaaaatcaa acttacacac ggtgtcatca aagatcagtt 49740gcagagcaaa aacgggtacg cggtccaata cttgtacgcg acgtttctca acacggcctc 49800gttctacgcc aacgtgcaat gtttaaatgg tgtcaacgaa attatgccgc cgcggagcag 49860cgtaaagcgc tattatggac gtgatgtgga caacgtgcgt gcatggacca cgcgtcatcc 49920caacattagc cagctgagta cgcaagtctc ggacgtccac attaacgagt catctaccga 49980ctggaatgta aaagtgggtc tgggaatatt tcccggcgct aacacagact gcgacggtga 50040caaaaaaatt attacatttt tacccaaacc taattcccta atcgactcgg aatgcctttt 50100gtacggcgac cctcggttta atttcatttg ctttgacaaa aaccgtttgt cgtttgtgtc 50160acaacaaatt tattatttgt acaaaaatat tgacgcaatg gaggcgttgt ttaaatctac 50220accattggtt tacgcgctgt ggcaaaaaca taaacatgag cagtttgcac agaggctaga 50280gatgttgttg cgtgattttt gcttaattgc cagttcaaac gctagttatt tactttttaa 50340acagcttaca cagctcatag ctaacgaaga aatggtgtgc ggagatgaag aaatattcaa 50400tttaggcggc caatttgtag acatgattaa aagcggtgct aaaggcagtc aaaatctgat 50460taaaagcacg caacaatacc gacagacttt aaatacagat attgaaactg tgtcttcacg 50520agccaccacc agtttaaata gttacatatc ttctcacaat aaggtaaaag tgtgtggcgc 50580cgacatatat cataacacgg ttgtgttaca gagcgtgttt attaaaaata actatgtttg 50640ttacaaaaac gacgaacgta caatcatgaa tatttgcgct ttgccctctg agtttctgtt 50700tccagaacat ttgctcgaca tgttcattga atgataatat aaatagagcg catttgattg 50760catgcaatca gtgttttatt aattttagag caacatgtac gataaattta tgatctatct 50820tcacttgaat gggctgcacg gagaagcaaa atactacaaa tatttaatgt ctcaaatgga 50880ttttgaaaat caagtagccg atgaaatcaa gcggttttgt gaaactcgtc tgaaaccggc 50940aatcagttgc aacactttaa ctgcggaaag tctcaatacg ctcgtagaca gcgtagtctg 51000caaaaatgga ctgttaaatc cttacgccaa agaagtacag tttgctttgc aatatctttt 51060tgacgatgac gaaatatcca aacgagatca agatggcttt aaactatttt tattacataa 51120ttatgacagg tgtgaaaata tggaagaata ttttttaatt aacaatttta gcatagcaga 51180ctacgaattt gaagacatgt ttgaaattgt tcgtattgat tgtagagatc tgttattact 51240tcttgctaaa tataatatgt aattaaaatt ttgtttgttt tattaaaatc ctggattaaa 51300aaatgacgaa taatttgatt tgcgtgcacg ccaacaagat tcttcgtcat tatgatcaat 51360gcgtgcatca agtttatgct tttgtaattg gcttctgacc actttagcca tttgagcgta 51420tctgcattcg tcgtctagag tttcaaacac cagatcggcg caattataaa atccttcacc 51480cacgggatct atgcgctgcc aacgcacata cattacaaat tgatttgacc tgtacggtat 51540tactacgggt atagaataga ctagactgtt gtcacataat gaatcgcccg gatttggaat 51600taaatttgaa tcgttaccac ctatgtattc taattcgttc caagttattg gattgcgacg 51660atcccagttt gatttagtaa taaacacttc aaaataactg ggctcgtgta tggctgttgg 51720acaaaaatga acattcatct gataaaccgg ttgatagcga tttaaatata gcgtatttgg 51780cctccagttg ttaaaaggtt cgtccattcc gcttttatca ccaaacacag aattgcgatc 51840gtttgaaccg gcaccgcaaa gtgtgtgcgg cacaaccctt tgtttgatta ggtcaaaatc 51900gtcataatta ggaccggcca cagccgcgta ttccatatac tgttgaaaca tgtattgcgc 51960tgtggaagcg gccgccccgg attctaaatc gagagctcga tatttataat agactgattt 52020gtaagcattg cggcacgcgg cgtcgggaat gttatcgcca ttgtcgggcc aataaaagtt 52080tccatcttta aaacatttat attgacgggc cgtcggcacg gacaaatagc cgtgagagcg 52140cactgccggc gcgtgaatcg cagcaaacaa tgcaattaat aatgcaatca ttatgattat 52200acttatagaa cactaatcgg aataataacc gctgtcgtaa tcttggtcaa aaacgttatg 52260ttgaaacata ataacacctt acagtaacat acaataaaac aacatagtat cgtatataat 52320tataaacttt attttttcat tttatacaaa caaaatttat acgtattgtt agcacattga 52380gtgtcatttt cgctgtctga actatcacaa tcatcgtcat catcatcatc attgtcatcg 52440tcgtcgtcac gtttgcgttt gacactgcat tttttttggt taattttcac taacactggt 52500tcttttcgat cgtacaattg attctgcatg tacttttgca tgatcgcggt aaaacacttt 52560gcaattttat ccttttgttc gtcgccaaat atttccagca actcgttcat aaatgtgcac 52620aaaatgccca tgtgttttat ccagctgatt cgcattttca ctggatcgaa caaacgcaag 52680gggtacgctt tttctgttac cttgccttcg atgtctatca aaaggtacgg gatacgatct 52740ccgttgccgg gcacaaaatc cgtgcctttg ttaaccaaaa tttctctaca atgcctagcc 52800accgtaatca cgcgtctttt gggtgacgga ccctcattat cgtcagttga tttgcgtttt 52860ttgcccgggt tatcgttata ggtcatacta aagctgtagt cggtcaacga ttttgatttg 52920gcaaactcat catagtattc ataaaaacta gtctgtaaac tttgcaaaca tttgtccatg 52980tccaaatgac gcaatatttg ttccactgcc gtcctaaacg cgattctcat aaaaacgggc 53040atatcctttt taactaacca acccttgtat acgattttat tctcactgtt gagatagcaa 53100tattttttct tttttaatag tattaaaact ttcattaaat tttcaaatgc cattttgtaa 53160ccgtccgtga atgagttatt aacgcgtgtc tcaacatgtg tgcatatttg ttttaatgtg 53220tcggtttcgt tggatatttc gttatagtta aatgtgggca aaacaaatgt agaatctgtg 53280tcgccgtaca caactttaaa agtgatgctg cccagattga atttttctaa aatctcaggg 53340tcgttgctca aaccttcaat cagagaaatg gccagccgca actgattgcg accaactcta 53400gtgatgtagt ttgcaagcac tttgtaaaaa atgccataat aaccgtatat gctattggcg 53460gtgcgcttca cggaattttg tttttgatcg tacagatcgt acaagaatgc cgattcgctt 53520tgattgtcgc gattcttttt aaatttgcac ctttcgctta acaattttaa tagcaattta 53580acaactattg cacgcgaatt gtggttcaaa tacacgttgc cgtcttcgca taaaattaaa 53640ttggacaaac aagcacaaat ggctatcatt atagtcaagt acaaagaatt aaaatcgaga 53700gaaaacgcgt tcttgtaaat gcctgcacga ggttttaaca ctttgccgcc tttgtacttg 53760accgtttgat tggcgggtcc caaattgatg gcatctttag gtatgttttt tagaggtatc 53820aattttcttt tgagattaga aatacccgct gcggctttgt cggctttgaa ttggcccgat 53880attattgaca gatcgttttt gttaaaaaaa tacgggtcag gctcctcttt gccggtgctc 53940tcgttaatgc gcgtgtttgt gatggctgcg taaaagcacg ccacgctaat caaatgcgaa 54000atattacata tcacgtcgtc tgtacacaaa cgatgcaata tacattgcga atatacagaa 54060tcggccattt tcaatttgac aaacaatttt atcggcaaca tgcaatcctg cacgttgtac 54120ttggcaatca cgtccagccg tcgagtgttg tacatcttga ccatttcggt ccaaggcaaa 54180tcgattttgt tttcacccaa atagtaacta ctgattgtgt tcaattgaaa gttttcaact 54240ttatgctgat tagaatcgct gctgaaaaat ttatacaaat caatgtgaat gtaatagtta 54300aaataatacg tgtccacttt gttgcccaac ttgtttataa acagctttgt cgtcggcgcc 54360gcagccggca aatcgtaacg ctttaatagc attttggttt tattcaatcg tccaagtata 54420tagggcagat caaatacgtc tccgttaaaa tccaaaatca catcgggatt tgtaattttt 54480atcatgtcaa aaaacgctgt aatcatgtcg atttcatttt gaaacatgac cacatacgtg 54540tcatcgtcat aggtctctgg aatctgggtc ggcagcttgt gatacataaa acaaaatttt 54600gcatactcgt cgtttttgta caccacaaat cctatagaca ttatgcaatc aaccgatgct 54660ttcgacatgt tgtggccgtc cgaatgagtc tcaatgtcat agcacgacaa aacgggcatg 54720atgccgctgg ttaaagtcat ttcatcgacc aactcaaagt cttcattaaa atgttgcaaa 54780ttaaacatgc gcgtcgtcga tccaccgaca tagttatttt ggcagcgttg tgttttcttg 54840aatcgcatat aggcgccttc cacaaacggc gtttgcatgt gtacgcgatt aacgttgtga 54900agaaacttgt ccaaacacgc cgcgttgtcc gatggcgctg ctttgtttct ttcgtattta 54960atcacgttta tcttgttcaa ataatttcct tccacgcccg gcgccacaaa cgtggtgtag 55020ctgatgcact tgttgcggca agacggaaat atgtgcttgt cgtagcattg tttgtaagaa 55080tacaaattta gttttacttt aaagtaaaac tgcagcactc gttctttgat atttgtatta 55140caaaatgcaa acaagcaacc ttgtttttca tcgtaatgca aacgaatgat acgaaacgta 55200tcggctgaag taatattgaa ttctcctggt tttgcatatt ctgcaaagcg cgttttgagt 55260tcattgtaag gatatatttt catttttaaa tatgcagcga tggcccaaat atggaggcac 55320agacgtcaac acgcgcactg tacacgattt gttaaacacc ataaacacca tgagtgctcg 55380aatcaaaact ctggagcggt atgagcacgc tttgcgagag attcacaaag tcgttgtaat 55440tttgaaaccg tccgcgaaca cacatagctt tgaacccgac gctctgccgg cgttgattat 55500gcaattttta tcggatttcg ccggccgaga tatcaacacg ttgacgcaca acatcaacta 55560caagtacgat tacaattatc cgccggcgcc cgtgcccgcg atgcaaccac cgccaccgcc 55620tcctcaaccc cccgcgccac ctcaaccacc gtattacaac aattatccgt attatccgcc 55680gtatccgttt tcgacaccgc cgccaacaca gccgccagaa tcgaacgtcg cgggcgtcgg 55740cggctcgcaa agtttgaatc aaatcacgtt gactaacgag gaggagtctg aactggcggc 55800tttatttaaa aacatgcaaa cgaacatgac ttgggaactt gttcaaaatt tcgttgaagt 55860gttaatcagg atcgtacgcg tgcacgtagt aaacaacgtg accatgatta acgttatatc 55920gtctataact tccgttcgaa cattaattga ttacaatttt acagaattta ttagatgcgt 55980ataccaaaaa acaaacatac gttttgcaat agatcagtat ctgtgcacta acatagttac 56040gtttatagat ttttttacta gagtctttta tttggtgatg cgaacaaatt ttcagttcac 56100cacttttgac caattgaccc aatactctaa cgaactttac acaagaattc aaacgagcat 56160acttcaaagc gcggctcctc tttctcctcc gaccgtggaa acggtcaaca gcgatatcgt 56220catttcaaat ttgcaagaac aattaaaaag agaacgcgct ttgatgcaac aaatcagcga 56280gcaacataga attgcaaacg aaagagtgga aactctgcaa tcgcaatacg acgagttgga 56340tttaaagtat aaagagatat ttgaagacaa aagtgaattc gcacaacaaa aaagtgaaaa 56400cgtgcgaaaa attaaacaat tagagagatc caacaaagaa ctcaacgaca ccgtacagaa 56460attgagagat gaaaatgccg aaagattgtc tgaaatacaa ttgcaaaaag gcgatttgga 56520cgaatataaa aacatgaatc gccagttgaa cgaggacatt tataaactca aaagaagaat 56580agaatcgaca tttgataaag attacgtcga aaccttgaac gataaaattg aatcgttgga 56640aaagcaattg gatgataaac aaaatttaaa ccgggaacta agaagcagca tttcaaaaat 56700agacgaaact acacagaggt acaaacttga cgccaaagat attatggaac tcaaacagtc 56760ggtatcgatt aaagatcaag aaattgccat gaaaaacgct caatatttag aattgagtgc 56820tatatatcaa caaactgtaa atgaattaac tgcaactaaa aatgaattgt ctcaagtcgc 56880gacaaccaat caaagtttat ttgcagaaaa tgaagaatct aaagtgcttt tagaaggcac 56940gttggcgttt atagatagct tttatcaaat aattatgcag attgaaaaac ctgattacgt 57000gccgatttct aaaccacagc ttacagcaca agaaagtata tatcaaacgg attatatcaa 57060agattggttg caaaaattga ggtctaaact gtcaaacgcc gacgttgcca atttgcaatc 57120agtttccgaa ttgagtgatt taaaaagtca aataatttct attgtaccac gaaatattgt 57180aaatcgaatt ttaaaagaaa attataaagt aaaagtagaa aatgtcaatg cagaattact 57240ggaaagtgtt gctgtcacaa gtgctgtaag cgctttagta cagcaatatg aacgatcaga 57300aaagcaaaac gttaaactta gacaagaatt cgaaataaaa ttaaacgatt tacaaagatt 57360attggagcaa aatcagactg attttgagtc aatatcagag tttatctcac gagatccggc 57420tttcaacaga aatttaaatg acgagcgatt ccaaaacttg aggcaacaat acgacgaaat 57480gtctagtaaa tattcagcct tggaaacgac taaaattaaa gagatggagt ctattgcaga 57540tcaggctgtc aaatctgaaa tgagtaaatt aaacacacaa ctagatgaat taaactcttt 57600atttgttaaa tataatcgta aagctcaaga catatttgag tggaaaacta gcatgcttaa 57660aaggtacgaa acgttggcgc gaacaacagc ggccagcgtt caaccaaacg tcgaatagaa 57720ttacaaaaat ttatattcat tttcatcttc gtcatacttc aacagtccca acacgttcat 57780gttgtgattc tcgccgttct cgacagttac gtaaatagtt actttgatta aattatcttc 57840cagcagcatt gagatttgat tgaaatccgc acatagcttt tgtagcgaat ccgcttcggt 57900ttttttattt gtgttgacgt agaaaacaga tttgttccat ttgcccaagt cggaagaggt 57960agaacagtca tccgaatcgg caatgttcaa ctcgtcgctt ttaaactgca caataaactt 58020gttatcgccc atgtcatttt cttccaattc gctttttaac acatttacat tgtacgaagc 58080aacgtgtttg ttcgatcgac taatgttgat ctttgcgttt gtgcaatttt gcaaatttga 58140atatgcttcg ctttctttag cctcgcacaa ttcgatgcgc gtagagttga ccacgttcca 58200attcatgtac acgtttgatc cattaaaaat ttgttgacac tttatactgt aaatggtaaa 58260gatttggttt tcattgtctt ttaaatattt aaacacctca ttgatgtcgt cagacccctt 58320tatattgttc ttgaatagat ttattagtgt tttcgcattg acagaacatt ccacttgaac 58380cacgtcggga tcgtcgttga gatttttgta cacaacctca aaaacaactt tgtacaaacc 58440gctgttgatt ttcttgtaga taaatttgta ctttacaata atattgacgc catcttcatt 58500ttcaaaatgt ttgttagtca aatagtcgct catgggggtt gcagtttcaa tttccatttc 58560acattctttg tattcgttga tctgaatcat ttgactaaac tttgttttca cataatttaa 58620actaatgtca tagcacttgc cttcttccat gtctttgaaa gattgcgaat cgccgtagta 58680ttcttgaatt ttgttgtcgg acattattcg aaaagtgtaa tggtattcat tatcgatact 58740caacgtcatt ttgctcatca atttaccact aatccttttg taattttctc taatcttctt 58800ggggctactg gccatagcca tgcgttttat aagcggctca ccgctacttt ctccagacaa 58860agatcttttg gtcgccatat tgctgttgtc gatatgtggg aatctatccg atggcaaata 58920ctgaatggcg acgaaatcga agtgtcgcca gagcaccgtt cgttagcgtg gagggagttg 58980attataaacg tggccagcaa cacgccgctc gacaacacgt tcagaacaat gtttcaaaaa 59040gccgattttg aaaatttcga ctacaacacg ccgattgtgt acaatttaaa aacaaaaact 59100ttaacaatgt acaacgagag aataagagcg gctctgaaca gacccgtccg atttaacgat 59160caaacggtca atgttaatat tgcgtacgta tttttgttct ttatttgtat agttttgctg 59220agcgtgttgg ccgtcttttt cgacacaaac attgcgaccg acacgaagag taaaaatgtt 59280gcagcaaaaa ttaaataaac tcaaagatgg tttgaacacg ttcagcagca agtcggtggt 59340ttgcgctcgc tcaaaattat ttgacaaacg cccaacgcgc agacctagat gttggcgaaa 59400actatcagag atcgacaaaa agtttcacgt ttgccgacac gttgacacgt ttttggattt 59460gtgcggcgga ccgggcgagt ttgccaacta taccatgtcg ttgaacccgc tttgcaaagc 59520gtatggcgtc acgttgacaa acaactcggt gtgcgtgtac aaaccgacag tgcgcaaacg 59580caaaaatttc acaaccatta cggggcccga caagtcaggc gacgtgtttg ataaaaatgt 59640tgtatttgag attagcatca agtgtggcaa cgcgtgcgat ctggtgttgg cagatggctc 59700ggttgacgtt aatggacgcg aaaacgaaca agaacgtctc aactttgatt tgatcatgtg 59760cgagacgcag ctaattttaa tttgcctgcg tcccggcggc aattgcgttt taaaagtttt 59820cgacgcgttt gaacacgaaa cgatccaaat gctaaacaag tttgttaacc atttcgaaaa 59880atgggtttta tacaaaccgc cttcttctcg gcctgccaat tccgaacgct atttaatttg 59940tttcaataaa ttagttagac cgtattgtaa caattatgtc aacgagttgg aaaaacagtt 60000tgaaaaatat tatcgcatac aattaaaaaa cttaaacaag ttgataaact tgttgaaaat 60060ataacgtgtg tataaaaagc cagcggcttc aaatcaggca tcattcaaca tggattcgct 60120agccaatttg tgcttgaaaa ccctgcctta caagtttgag ccgcctaagt ttttacgaac 60180aaaatattgc

gacgcatgtc gctacagatt tttaccaaaa ttttctgatg aaaaattttg 60240tggacaatgc atatgcaaca tatgcaacaa tccaaaaaat atagattgtc catcatcata 60300tatatcgaaa attaaaccga agaaagaaaa caaagaaata tatattacca gcaacaagtt 60360taataaaacg tgcaaaaacg aatgtaatca acaatcaaac cggagatgtt taatttccta 60420ttttacaaat gaaagttgta aagagctcaa ttgttgttgg tttaataaaa actgttacat 60480gtgtttggaa tataaaaaga atttatacaa tgtaaatttg tatacgattg atggtcattg 60540tccttcgttt aaagccgttt gtttttcatg tataaaaaga atcaaaacgt gccaagtttg 60600caatcaacct ttattgaaaa tgtacaaaga gaagcaagaa gagcgtttga agatgcagtc 60660gctgtacgca acgttggccg atgtagattt aaaaatatta gacatttacg atgtcgacaa 60720ttattctaga aaaatgatat tgtgtgctca atgtcatata tttgcacgct gtttttgtac 60780caataccatg caatgttttt gtcctcgaca gggttataag tgtgaatgta tatgccgacg 60840atctaaatat tttaaaaata atgtattgtg tgttaaaagt aaagcggctt gttttaataa 60900aatgaaaata aaacgtgttc caaaatggaa gcatagtgta gattatactt tcaaaagtat 60960atacaagtta ataaatgttt aattttaagg atattgttat ggaataaact ataaaatgaa 61020tttgatgcaa tttaattttt tgatactttc cacagacggt agattcagaa cgatggcaaa 61080catgtcgcta gacaatgagt acaaacttga attggccaaa acggggctgt tttctcacaa 61140taacctgatt aaatgtatag gctgtcgcac gattttggac aagattaacg ccaagcaaat 61200taaacgacac acgtattcga attattgcat atcgtcaacc aacgcgttga tgttcaatga 61260atcgatgaga aaaaaatcat ttacgagttt taaaagctct cggcgtcagt ttgcatcaca 61320atccgtggtc gttgacatgt tggctcgtcg cggcttctat tattttggca aagccggcca 61380tttgcgttgt tccggatgcc atatagtttt taaatataaa agcgtagacg acgcccaacg 61440ccggcacaaa caaaattgca agtttctcaa cgcaatagaa gactattccg tcaatgaaca 61500atttggcaaa ctcgatgttg cggaaaaaga aatactggct gccgatttga ttcctccgcg 61560gctaagcgtt aaaccttcgg cgccgcccgc cgaaccgcta actcaacagg tctccgaatg 61620caaagtttgt tttgatagag aaaaatcggt gtgtttcatg ccgtgccgtc acctggctgt 61680gtgcacggaa tgttcgcgtc ggtgcaagcg ttgttgtgtg tgcaacgcaa aaattatgca 61740gcgcatcgaa acattacctc agtaaacatt gcaaacgact acgacattct ttaaaaataa 61800gctatatata aatattgcat tgtatgacaa aaaaattatt aacctactgc aaagtaaaac 61860ttgtaaaagg cttttcaaaa aaatttgcga gtttattttg tcgctgcgtc gtgtcgcatc 61920taagcgacga agacgacagc gacggtgatc gctattatca gtataataac aattgtaatt 61980tcatatacat aaatattgta aaataaaaga catattattg tacataatgt tttattgtaa 62040ttaaattaat acaccaattt aaacacatgt tgatgttgtt gtgaataatt tttaaatttt 62100tacttttttc gtcaaacact atggcgttgc tttcgattag ttttttcgtt agcatttcat 62160ctaaaaaatc aaactgtttg cccggcgcgt ttagggattc tatggtgtag tcgggcgtgt 62220cgctgtttag atattggtcc acttcgcgca ttatgtccaa gacgttgttc tgcaaatgaa 62280tgagctttgt caccacgtcc acggacgtgt tcatgtttct tttttgaaaa ctaaattgca 62340acaattgtac gtgtccacta tacaattcgg cttaatatac tcgtcggcgc aatcgtattt 62400gcaatccaat ttcgtgttca acaaattggt gatgatatct ttgaacgtgc acgttttcaa 62460tttgtcctta tcggccaacg caagtttcaa ttcgctctgt aaagtttcta aaattttgtc 62520tttattgttg tcaaattcgt gcgtgttgcg ttccaaccac aatttgaacg gctcgtcgac 62580aaaaatgctg cgcaacacct cgtacaactg tctgcctaac gtgtacactt gctcgtattc 62640tttcatgctg acctctttgc taacgtacat tactaaaaaa tctacaagta ttttcaaaca 62700tttgtaatag gcgacgtatt ttgatttaag ttttaaaccg tccaccgtgt attcgtccac 62760gttcgcatcg accacttttc gattattatc gccgcttgtt gccggcgcgt cggcctgttc 62820ggttttaact atatccggtt caatatttaa agtttcaaaa gatttaatgg cattcataaa 62880atcatctttt tgctttggcg tggtcaatgg taaatctatc gaggagttgt cgtccgtgtg 62940ctcttcgggc acgctgttca gacgtaacgt aatctttttg ggatcgtctt catcgggtat 63000caaatcggct ttaattttat tagaattgag caacgacatg gtggtcgctt gtaaatttaa 63060taaattaatt aaagactgaa attgtatatt gcacaaattt attttcattt ttattgatct 63120tactattaat acgctggcag ttggtatgct tcatccattt ttgtgactag aaaatttgct 63180aaaaaactga gctcgtcctg tgttaaaacg ttgtcgtcca cgaatctatg caatgtaaat 63240gttacactga cattgtttaa caatgcatgt attaaaaaat caacctgtcg cctactgagt 63300ttattagaag agtcgaccgt ttctactagt ttgtagattt tgttattttc aatttcattg 63360tttaaaaaca tgttaactac tcgtttgagt ttaagcgaaa aatccttgtc cggatagact 63420tgttcgcaca gccaattgct aagagtggtt ttgaccacgg acaccttggt ggtgaacgtc 63480gtcgatttga ccagttcggt gaaaaagttt ttcattaaat tggacatttt aacaaacact 63540tatcaatcta ttgagctggt atttttgttt agaatcgcat caagcgcttg ctcgatctcc 63600aatttttttc ggacgctctt agctttatga ctcggtatgt cttctacggt agactcggtg 63660ttcttactta taatggccgg gctgacgata ataaacacga gaaacaatat gagcagatac 63720aaaaagatgc tgttttcctt tttgtcatac actaggctaa atatggccag tgcgcccaac 63780aacaaatata aattcatttt tattccctta ctctattcgt tgcgatagta caacaacgat 63840tctcccgacg aaccggacga attgcgatta tgctgcgcgt cgtcgtcgtc gttgttgttc 63900tcctcttcgc tgctcgtttc gtctaaacct atattgtatt tgttcaagta atgtttggtg 63960cttgcggagg attcgtggtt cattaatttg gccacttttt gtaaaggcac gccgctattg 64020tataggttac tgctcaaata atgtcttatc atgttgctgc gcggccgttc catctcgacg 64080cccgactctt caaggagtcg cctgaaatct ttgaagggcg tcgaggtgtt tttagatatt 64140tgcaaaatgg tcgggtttcg tgaataaatc tcgcgtgcca attccaacgg tttcattttg 64200atgttgttga gtgtgttatt acgactgcgt tttcgcttta aattaatcgt gtcgctgtgc 64260agttttcctc ttttaattag cacgttgaga tcgtccacgc tgagttggcg cgcttcgttg 64320attcgcatac ccgtccctaa catgatgcaa aacactatcg cgcccctaat tagaccgcgg 64380tcgtgaacat aatcgctgtt gagcatttta attttatcat taataaaatt taatatggta 64440tctattacgt ttttaagcat taaattcttt tccttttccc tgatattttt gagctccttg 64500tcgcgcggca gcataaccat gcggggaatt ttgtattcgg gcaagttcat catgttggtg 64560taaaagttta tagtcaactg tagtgtttct ttggtgaccg agcgaagttc gagcatgcgc 64620ctgcacagtt cttggggatc aatgagaagt gtttggtttt ctatcgagtc aaactccttg 64680tccaacgagt acgacatgtc ttccaggtga acatcgtcta ccgagcagta cacaatttta 64740atgaatcgag acttgtaact ttttaaagtg gtgggcgcaa acggtttggg gaacatgtac 64800ttgctccaca gactgttgtt tttcacctcg tcgggcgtgc atcgttgccg atcggtggcc 64860aaatcgaaca cggactcgaa ccggggagcg gattgaattt ttattttcca agaattaaaa 64920ttgttttcgt tgcgaacatt aaaaccgttc attgtggtta atcaaattta ttaaaaacaa 64980aaggagaatc ggtgtcaata ctatccgaat attgttgttg ttctcttaat attacgaaat 65040aatatattac atacagcagt aagaataaag ctataaaagc gactacacta attaaaatta 65100taattcccgc cgacacgttg ctcgtcgtgt tgtcatagcc caccatgtcg tttattggca 65160ttttgtgaac gggctcgcta aattgttgcg gttcgctggc agtatcgtcg ttgagcgcca 65220atttcaacgg gatgtattcc accttttcgt ggttgcccaa ccgatagtag ggcacgtcca 65280aattcatgtt tacaacttat ttgctaacag gaatttatgc aacaaaagtg gtttggcttt 65340gatgagacgc aatttgaaat acttgctgca tttacgctta agattgtatt ccatgcgggc 65400ggcggtgttg tagtcgtacg cgctcgcgct gtgatacacg agccgtaaat tggttgcgtt 65460gcgcaaacac ttggcgcctt gtttgttcga atgctgtttt atgcgtctgt taagattgct 65520cgtgatgccc gtgtacaatt ttccattgtc ttgccgcaga atgtacacgc accacacctt 65580gttggtgtac agagtcgtcg ccatgattat gcagtgcgcc ctttcgtgtt cggccgagtg 65640gcgttaggcg cagccgcggc aataatcgcg ttggcgtcct tgttgtaatt tatttgttga 65700aaaataaaac gtcttagagt ttcgttttgg aacgccaatt cggtcaagct ctcctggcaa 65760gcgcttttgg tcaaatgagc ggccggcgaa ttgaccgcgt tggcggccga cgttaagaag 65820gtggcgttct ggaacatgct gggctgcttg ccggctcgcg tcgccagctc ggccatgtaa 65880ttgaatatgt tggcagacgc agatagcggc gccaaaaacg caacgttctc ttttaaactc 65940atgactcgcg ccctgttttt ttcgttcagc acgtagtggt agtaatcgcc gccgccggca 66000aacagatcgt caatcacggc gttgatcaga tcgttgatca tgttgatgtg cggaaagcga 66060cgcgactcga ctgcgctctg tatgtttggc ggcagagtgg cgtgcttgag caacagagtc 66120atgtaattgt tggccagctg ctgattgaaa ggtaacggaa tgggaatgtt gcacgtcacc 66180gcttccgcca ccatgtactg gacggccaga ctgagttgtt tggcggcctc ggccaaagcg 66240tctttgccca acatatcagc gccaccgttg taaaactttt gcgcgtacgc cggcagcgaa 66300tttagcacaa acgatggctg aaatatattt gaatcgctcg acagggactc ggccgcgttg 66360ctctgtccca actctttttg caaccgaatc aggtggcgta tcatggtttc ctccgattca 66420aaccgcttta ccacgtttac gctgattggg ttcgtgtcga tgcacatgtc acgaatagtg 66480tttataaaaa gaatcatgag aggactaagt tctgacatgt cattgcacct gtaatatcta 66540ataatctttt gaacaaaatc cacacatttg ttgtaccaaa tagattcacc ggcgtcgagc 66600gtcggttctt tgctcttgtt gtacggtgca atcgctaccg agtttgtgct gttgctgcgg 66660ctcgtgtaat ccatcctgtt gtcgcgcgtg gcgacggtcg taggcaccgt cgccggcggc 66720acgtacccgg gcgcgttgta agtttgcgcg ctggtgaata tggccgttgc cggattagag 66780ggatacctca gcggcggagg ggtgttgtaa taaaaattgc cacgttcatc tgtcatactt 66840tttatttgta ctcttatgat tacaaaactc aatatacgga ttacttataa tatagttgtt 66900gtgacaaaaa agcgataata aaattaacaa aattatcaac aagttaatca tggaaaattt 66960ttcaacgttg aataacaaca acaaaatggc gcaggtcaac agcaccgttt gaaaactgac 67020gcgccgacac aaaatgcttt cgcaatttct aaaagccaca ttaaacgaat tttcaccttt 67080gatataatca cgcagttctt ttttacaaca ttcgtcgcac aaaattaaca cctttataat 67140gaggccgtcg gtgtgtatcg tttgaaatgt ccgcggttga ctgcctggat gaaattcaaa 67200cgagtaccca gtggacacgt gtatctgtgc aaaataatgg gctaatatcg aggcgcccgt 67260ttttttaacc tttacttttg atattttaat aacattaatg ttgttatttg cgtaatcaga 67320gtttttattg tggtgatcat cgtacaaata atgaagcaac agttcactat cgtatttaat 67380cttgtttagc gttgtcaagt ttttgtttct taggcgttgg agcgtctccg tcgtcgatat 67440tttcttcgaa atcgagtcca acaacgtcgg cgtttccttc ttgctcatcg atagcggcgg 67500cggaggcggc ctctccgtcg tcgtcattcg cggtttctac agtgcgtttg ggcgacgacg 67560tgtgtacagc agcgtccgtc ttactattat cggaccgcca aatttttgtt tgaaataaca 67620tttggccctt gttcaacttt atttcggcgc agttaaacat tattgcatta agatcatatt 67680cgccgttttg caccaaattg cacaaaacac catagttgcc gcacgacact gtagaatagg 67740cgtttttgta caacaatctg agttgcggcg agctagccac cttgataata tgggcgccaa 67800cgccccgttt ttttaagtaa tattcgtctt caattataaa atctagtacg ttttcatctt 67860cactgttgat ttgggcgttc acgatgatgt ctggcgtaat gttgctcatg cttgccattt 67920ttcttataat agcgtttact ttaatgtatt tggcaattta ttttgaattt gacgaaacga 67980ctttcaccaa gcggctccaa gtgatgactg aatatgtgaa gcgcaccaac gcagacgaac 68040ccacacccga cgtaataggc tacgtgtcgg atattatgca aaacacttat attgtaacgt 68100ggttcaacac cgtcgacctt tccacctatc acgaaagcgt gcatgatgac cggattgaaa 68160tttttgattt cttaaatcaa aaatttcaac ctgttgatcg aatcgtacac gatcgcgtta 68220gagcaaatga tgaaaatccc aacgagttta ttttgagcgg cgacaaggcc gacgtgacca 68280tgaaatgccc cgcatatttt aactttgatt acgcacaact aaaatgtgtt cccgtgccgc 68340cgtgcgacaa caagtctgcc ggtctttatc ccatggacga gcgtttgctg gacacgttgg 68400tgttgaacca acacttggac aaagattatt ctaccaacgc gcacttgtat catcccacgt 68460tctatcttag gtgttttgca aacggagcgc acgcagtcga agaatgtcca gataattaca 68520cgtttgacgc ggaaaccggc cagtgtaaag ttaacgaatt gtgtgaaaac aggccagacg 68580gctatatact atcatacttt ccctccaatt tgctcgtcaa ccagtttatg cagtgcgtaa 68640atgggcgcca cgtggtgggc gaatgccccg cgaataaaat atttgatcgc aacttaatgt 68700cgtgcgtgga agcgcatccg tgcgcgttta acggcgccgg acacacgtac ataacggccg 68760atatcggcga cacgcaatat ttcaaatgtt tgaataataa cgagtcacaa ctgataacgt 68820gcatcaaccg gatcagaaac tctgacaacc agtacgagtg ttccggcgac tccagatgca 68880tagatttacc caacggtacg ggccaacatg tattcaaaca cgttgacgac gatatttcgt 68940acaacagtgg ccaattggtg tgcgataatt ttgaagttat ttccgacatc gaatgtgatc 69000aatcaaacgt gtttgaaaac gcgttgttta tggacaaatt tagattaaac atgcaattcc 69060caactgaggt gtttgacggc accgcgtgcg tgccagccac cgcggacaat gtcaactttt 69120tacgttccac gtttgccatt gaaaatattc caaaccatta tggcatcgac atgcaaacct 69180ccatgttggg cacgaccgaa atggttaaac agttggtttc caaagatttg tcgttaaaca 69240acgacgccat ctttgctcaa tggcttttgt atgcgagaga caaagacgcc atcgggctta 69300acccgttcac cggcgagcct atcgactgtt ttggagacaa cttgtacgat gtgtttgacg 69360ctagacgcgc aaacatttgt aacgattcgg gaacgagcgt tttaaaaacg ctcaattttg 69420gcgatggcga gtttttaaac gtattgagca gcacgctgac cggaaaagat gaggattatc 69480gccaattttg tgctatatcc tacgaaaacg gccaaaaaat cgtagaaaac gaacattttc 69540agcgacgtat attgacaaat atactacagt cggacgtttg tgccgaccta tatactacac 69600tttaccaaaa atatactaca ctaaactcta aatatactac aactccactt caatataacc 69660acactctcgt aaaacggccc aaaaatatcg aaatatatgg ggcaaataca cgtttaaaaa 69720acgctacgat tccaaaaaac gctgcaacta ttccgcccgt gtttaatccc tttgaaaacc 69780agccaaataa caggcaaaac gattctattc tacccctgtt taaccctttt caaacgaccg 69840acgccgtatg gtacagcgaa ccaggtggcg acgacgacca ttgggtagtg gcgccgccaa 69900ccgcaccacc tccaccgccc gagccagaac cagagccaga acccgagcca gaacccgagc 69960cagagttacc gtcaccgcta atattagaca acaaagattt attttattca tgccactact 70020cggttccgtt tttcaagcta accagttgtc atgcggaaaa tgacgtcatt attgatgctt 70080taaacgagtt acgcaacaac gttaaagtgg acgctgattg cgaattggcc aaagacctat 70140cgcacgtttt gaacgcgtac gcttatgtgg gcaatgggat tggttgtaga tccgcgtacg 70200acggagatgc gatagtggta aaaaaagaag ccgtgcctag tcacgtgtac gccaacctga 70260acacgcaatc caacgacggc gtcaaataca accgttggtt gcacgtcaaa aacggccaat 70320acatggcgtg tcccgaagaa ttgtacgata acaacgaatt taaatgtaac atagaatcgg 70380ataaattata ctatttggat aatttacaag aagattccat tgtataaaca ttttatgtcg 70440aaaacaaatg acatcattcc ggatcatgat ttacgcgtag aattctactt gtaaagcaag 70500ttaaaataag ccgtgtgcaa aaatgacatc agacaaatga catcatctac ctatcatgat 70560catgttaata atcatgtttt aaaatgacat cagcttatga ctaataattg atcgtgcgtt 70620acaagtagaa ttctactcgt aaagcgagtt tagttttgaa aaacaaatga gtcatcatta 70680aacatgttaa taatcgtgta taaaggatga catcatccac taatcgtgcg ttacaagtag 70740aattctactc gtaaagcgag ttcggttttg aaaaacaaat gacatcattt cttgattgtg 70800ttttacacgt agaattctac tcgtaaagta tgttcagttt aaaaaacaaa tgacatcatt 70860ttacagatga catcatttct tgattatgtt ttacaagtag aattctactc gtaaagcaag 70920tttagtttta aaaaacaaat gacatcatct cttgattatg ttttacaagt agaattctac 70980tcgtaaagcg agtttagttt tgaaaaacaa atgacatcat ctcttgatta tgttttacaa 71040gtagaattct actcgtaaag cgagtttagt tttcaaaaac aaatgacatc atcccttgat 71100catgcgttac aagtagaatt ctactcgtaa agcgagttga attttgatta caaatatttt 71160gtttatgata gcaagtataa ataaccgcac aaagttaaat ttttttcatt tacttgtcac 71220catgtttcga atatacccta ataacacaac tgtgcccggt tgtttagtgg gtgacattat 71280tcaagttcgt tataaagatg tatcacatat tcgctttttg tcagattatt tatctttgat 71340gcctaacgtt gcgattgtaa acgaatatgg acctaacaac cagttagtaa taaaacgcaa 71400aaacaaatcg ctgaaaagct tgcaagattt gtgtctggac aaaatagccg tttcgctcaa 71460gaaacctttt cgtcagttaa aatcgttaaa tgctgtttgt ttgatgcgag acattatatt 71520ttcgctgggt ttaccaatta tttttaatcc ggctttgcta caaagaaaag tgccgcagcg 71580cagcgtggga tatttcatga attcaaaatt ggaaaggttt gccaattgtg atcggggtca 71640tgtcgttgaa gagaaacaat tgcagagtaa tttgtatata gattattttt gtatgatttg 71700tggtttaaat gtttttaaaa taaaagaata acaatttaca cattgtttta ttacatggat 71760aatgttgttt gtttgacatt aaaggttatc atggtgcaat gattaataat aaaacaatat 71820tatgacatta ttttcctgtt attttacaat ataaaatcac accaattgtg caaagtttta 71880ttatttgttt gtcgacggtc gaggggtcag cggcgtgtgc aacaataaaa aacatgaagc 71940tgttaacaat tttgatttta ttttattcat tttttatgaa tttgcaagcg ctaccagatt 72000accatcaagc aaataggtgt gtgttgctgg gaactcgcat tggatggaac gatgacaata 72060gccaagatcc caacgtatat tggaaatggt gttaaataaa agtgaatata ttttttataa 72120aattttttat ttaaaattcc aagtaatccc tgcaaacatt aaacactgta ggtattttta 72180aatcttgcca catgcgaaca acgcacggcc tgtcgtcgaa caccgctatt acattatatt 72240ttcctctgat atagttgtta aacaatttta attttaataa ataatcttta caagtatcgt 72300ctgaaggcct cataaacaat ttatatgatt taatatcaaa atacttttca atccagtttc 72360gagtgggctg ttcacaaatt acgcttctcc cgctcataaa cacgataatt gcgtcgtggc 72420aatttgccaa atacttaacg caagtaataa cgtctaagcg ggcttcatct tgagcaactc 72480tattatcaaa atcataaaac gatctatttg tgggcaaagc tactgtaccg tctaaatcac 72540ataatacagc gcggggaaat ttgtcgccga caggaacgta atattcgaaa ttatttacct 72600ttagaaactt tttatattgc tttttaatag tttctggatt taatggaaat ttatcagagc 72660gtttataatt gcgttcaaga gccgtttcca aagaaacgtc catcaaacgc gttaaaaaat 72720ggtaattatg cgttgcggcc attttttgcc acatgtccac cgattgagtg ttcaaattag 72780tgtcgctgac aaccacgttg gcaccacatt ttgcggcttt taaaaactgt tcaatgcaca 72840ttttggtaat ttgttcttct ttagtttgtc tacatttccg cgattggtta tagaaagcgt 72900tcagttttgt ataatcgccg tttaaaaaca acttaacgcg cacgtcgtct ctgttgattt 72960ctgtatagcc ttttaaactt ttggcatacg tgcttttgcc cgaacccgaa atgcctatca 73020acaccaacaa ttgttttgaa gaaggcaatt taattgttgg agcaagttta ttatttaatg 73080cctgcttagt cgatacaaat tttataatat ttttgatcat tttaattttt tcaggctcgg 73140ttaattttaa aaattcgctc tccacatcga tcgtttgtgc tttacgacat ctgtacgcta 73200aacatttcca cggcaaagtt tgcaccagtt cgttgaaacg ctgttgattc aaagtcaaac 73260ccgacaccat aatatttatt gtagactcgt tggtgaacgt gtttctagca tcaacgtacg 73320gtttaatgac actttttaaa tgcgggaaaa gagctagaaa gtcatcgtgt tcgccattta 73380taacaagctg cgccaattta gtaggatttt cagcacggct ctgatttttg tgcatgttca 73440aatacacgtc gcttttaatc ttgcatagtg gcgcgttgtt tttatcgtaa actacaaatc 73500cttcttccaa atttttcaac tgggccgcgt gttcgacaca ttcttgcaca gacgtaaact 73560cgtaacattt ggggtatttg caaaacggca aattggaaca gtaaaaataa tcgcccgttt 73620cgttgtttct gcttgccaaa taccacaacg ttggctgttc atcgtaaacg gttacaattc 73680tgttgtgttt gcttgttaac tcaaacatgt gagtcgacgc gcagtctaaa tattcgttac 73740acaacgcttg aaattgattg tgggcctcgt caagttgaag agcttgcaaa actaaacgtt 73800taaacgtcac gtctgacacg caaaggtttt ctgcaaaagc acttcctcgg gtgctggcat 73860gccattcgcc gttgtacttg tagattttaa ttaaacttcc gtcgattttt tcgtaaaact 73920taaaattctc cttcgattgg aacagtttgt gatgagcatc ttcgccgccg atattttgta 73980gcaattcttg aaaattaaag aaacgatcga aagaacgcga cacaacggcg tacgtgcggc 74040tgttaagaat taaaccgcga cattccacga ccacaggatg atctcgatcg cgttcaaacg 74100attcgtaatt aagaaccatc aaatcgtgtt cggtataatt tttaattttg actttaaact 74160tgtcacaaag atttttcact ccgccgtttg caagtagacg cgaaacgtgc aacatgattg 74220ctgtttaata atgcatacca atgctaaact gtctattata taaagtgcag tgataacttt 74280gttatcaacg cgttcgatgc cgacatatat aaacgcaatg taacagtttt tgctagtacc 74340atcgcataca acattatgaa tacaaggggt tgtgttaata ataataaaat gatatttatg 74400aatgctttgg gcttgcaacc tcaaagtaaa ttgaaaatta ttgcacataa aatactagaa 74460aaatgtaaac gtgacgcgta cacgcgtttc aagggcgtaa aggcgatcaa gaatgaacta 74520aaaacataca atcttacgtt gcaacaatac aacgaggcgc tcaatcagtg cgctttaaac 74580gatagccgat ggcgcgacac aaataattgg catcacgata ttgaagaagg tgtgaaaata 74640aacaagagac atatatatag agttaatttt aattctaaaa cccaagaaat tgaagaatat 74700tattacatta aagtagaatg ttatgtaaac agttaattaa tctacattta ttgtaacatt 74760tgtggtaata gtggcgttgg ttatacattt atatgattgt aatgttgtgt actcgttttg 74820taataaattt ttgtgtttaa tcaattcaat atttttattt gataaaacct tattttcgct 74880actcaatttg gcgtttttag acgcaagttt tgcgtaatcg tcattgagcg attttagcgc 74940cttttcagtt gtaattcgtt tcagttgcaa ttctttaaaa gatttatgca tgttgttgta 75000gtcgctttta attttgtcta acttttcttg catagaaacg cttgtttgtt gtaatttgtc 75060taaatctaat tgttgtttaa tgttgagctg cgtttgttcg gcaatgtcta cctgtagttt 75120ttttagtatc gcttgtgctt cagacagcat agtgtcgtcg gcatttgcgt tgttgtcttc 75180tgcgtcgtcc aacagacttt tttcaaacaa cacactggcc aaagaggccg catcaaaatt 75240agcgtttatt

ttattccatt gtgcgacact cgacgcgctg catttaatca catccacaac 75300gtttcggttt acgctgtaaa cgttgaaatg caaactttca accctacaca agggacatgg 75360tacttttttt cgttttctaa tcttgcgtat acacattgag cataattgat gtttgcacgt 75420gtctagttct aatacgggta ttatagtcaa tctgtctatt ggttgcagaa aataattttt 75480aatttctgca accgaaaaac aaatgttgca ttgcaattta acaaactcca tttttagacg 75540gctattcctc cacctgcttc gcctgcaaca ccaggcgcag gacctgccac tgcgccgccg 75600cccagagtag cgttaggatt tgctcttggt ataaagtcgt tgcgcaaaaa gttgttttct 75660gaattgatta tttggtatcc caaaaacagc ggaacgtacg tcgggtattc ttcgtatccg 75720ctaagcgttc tgtccagctc acgtgtgtcg ccttcaaatt tcaaaacgtt tctaatttgc 75780aaacgattgg gttgacttct cataatgtca ctgcttctta tcgggttgta caactcgggg 75840ccgtcgggca cagacgcgac cagacccgtt tcgtcaatta tacacgtggc gcaatttcta 75900aacctcaatt cctccgtgtc gatttgcaag tactcgggcg ctactgcgcg tcgaatcaaa 75960ttttgcaaaa atccactgta attgttaaat aattgatcgc cagcaccgcc tcgaagcgct 76020cgggcgttgg tcacgtcaaa gaaacgcaat tcgtctcgcg acacccgcga acaaaacgtg 76080ttcgggtttg tggtgtccag aatgcttttt gtagttgcgt aaacgctgtg tataacgcgt 76140tgcgtgttgc ttgtgaaacc ttcggtatat tttagattgt cgcatatagt gttaactgcg 76200ttttcgttgt tatatatcaa atgaaagatt agctgttcgg cttgcatcat actgtttaga 76260ttaaacacgt cttggtaatt ggttgcgctt ggaattaaaa ttcgcttgat acctctttct 76320ttatttccaa ctaaatgcct agcgatcgtc attttgaatt gattgtcgtc ttcgtcgaaa 76380atgggcaaaa ccatttttga cattttaaaa cgttttatga ggtggttgtt gcaaataaac 76440catccatcgt catgatacgc gtcgggcgaa cacggcgatt tgtatgttat gcacgcgtcg 76500aacgacacga tggacgcgaa aatgcagcga ttaactctca tttgtcgcgg cgccataccc 76560acgggcacta gcgccatatt gttgccgtta taaatatgga ctacggcgat tttgtgattg 76620agaaagaaat ctcttattca ataaatttta gccaagattt gttgtataaa attttaaatt 76680cttatattgt tcctaattat tcgctggcac aacaatattt cgatttgtac gacgaaaacg 76740gctttcgcac tcgtatacct attcagagcg cttgcaataa cataatatca agcgtgaaaa 76800agactaattc caaacacaaa aaatttgttt attggcctaa agataccaac gcgttggtgc 76860cgttggtgtg gagagaaagc aaagaaatca aactgcctta caagactctt tcgcacaact 76920tgagtaaaat aattaaagtg tacgtttacc aacacgataa aattgaaatc aaatttgaac 76980atgtatattt ttcgaaaagt gacattgatc tatttgattc cacgatggcg aacaagatat 77040ccaaactgct gactttgttg gaaaatgggg acgcttcaga gacgctgcaa aactcgcaag 77100tgggcagcga tgaaattttg gcccgcatac gtctcgaata tgaatttgac gacgacgcgc 77160ccgacgacgc gcagctaaac gtgatgtgca acataattgc ggacatggaa gcgttaaccg 77220acgcgcaaaa catatcaccg ttcgtgccgt tgaccacgtt gattgacaag atggcccctc 77280gaaaatttga acgggaacaa aaaatagtgt acggcgacga cgcgttcgac aacgcgtccg 77340taaaaaaatg ggcgctcaaa ttggacggta tgcggggcag aggtctgttt atgcgcaatt 77400tttgcattat tcaaaccgac gatatgcaat tctacaaaac caaaatggcc aatctgtttg 77460cgctaaacaa cattgtggcc tttcaatgcg aggttatgga caaacaaaag atttacatta 77520cagatttgct gcaagtgttt aaatacaaat acaacaatcg aacacagtac gaatgcggcg 77580tgaacgcgtc atacgctata gatccggtga cggccatcga atgtataaac tacatgaaca 77640acaacgtgca aagcgtcacg ttgaccgaca cttgccccgc aattgaattg cggtttcagc 77700aattttttga tccaccgcta cagcagagca attacatgac cgtgtccgtg gacgggtatg 77760tcgtgctcga caccgagttg agatacgtca aatataaatg gatgccaaca accgagttag 77820agtatgacgc cgtgaataag tcgtttaaca cactcaatgg gccattgaac ggtctcatga 77880ttttaaccga cttgccggag ttactgcacg aaaacattta cgaatgtgta atcacggaca 77940cgacaataaa cgtgttgaaa catcgtcgcg accgaatcgt gccaaattaa agcacgttaa 78000gcggatacaa cgggcagtcc gagctgttaa agtcaataca accatcgtta acaaacgaat 78060acgcattgtt gtgacagctg aggatataaa aaggaataga gaagtaattg caatgaaata 78120tcccgttaca attccacggc acagcgtatg ttgctcgagt tctatcagtt gcacacaacg 78180gcctaagaaa atttattaat gcttcatttg tatctatatt agaaggataa tacataggtt 78240cgcccaaagg actgggagaa ggcggcggcg aaggtgtagg tgtaggagga ataggagaag 78300gcggcggcga aggtgtaggt gttggaggaa taggagaagg cggcggcgaa ggtgtaggtg 78360taggaggaat aggagaaggt ggaggtgtag gtgtaggtgt tggaggtata ggtgttggag 78420gaggtgtagg tgtaggtgtt ggaggtatag gtgttggagg aggtgtaggc gaaggtggag 78480aaggtgtagg agtaggtgga ggtgtaggta acggtacaat tggtggagat gtaggtggtg 78540gtacaattgg tggatttgga tacaattcct gaatgtcgtc taatattttt aaagttaata 78600aaattattat aaataaattt aatattatta ttattattat tatcacaata atgtaccaca 78660tgttgcttaa atataaaaat taaacaaaga atgttgtatt attgcaaatt taacaatttt 78720ttgtattctc cccatgtcat gcgttcgtaa tgagcgggcg gttttttatt tctttgtatc 78780cacttgtaat cgttaatgtg gttgtgaaaa gtcatactga cgtaggccat taaatttttc 78840atgagcatat tatttgacac aactgcaaca tctgcgcctg ccgtttcttg ctggtacgaa 78900tcgacaaacg taatgtctgt gccgtatttt tctttgtcaa gtgcaatttc tataagctca 78960atgtggtaaa tgatgaaacc tttgacgttc atataatgat cgcggcacat ggcgcactgt 79020agtatgaaaa atacgttgta aaatagcacc ttcattgttt tcaactgctg catgacaaaa 79080tctaaactgc ttttgtctcg cgtatacacc atatcgtcga tgatgagact gagaaagtgc 79140atggtgtccc atatggtagt aaacgtgtaa gtaaaactct tgggctggca cgaacgcaaa 79200ttgagttctg tggttttgtc cataaattct atgcgaaact gttgcaagtc catgtcgggg 79260gatgcgttaa tggcccattc gatcaactgc tgcacctcgt acttttgaat gtctttgtat 79320ttcatcaaac acgcaaaatg gtataagtaa gttgcttgcg aagacaacag tttggtgagg 79380tgcgtcgatt tagaggctcg caaaaggtct atgagacgaa acgaatacaa cagatagctg 79440tctttgtaac gagaaaaaag cggcgtcagc ggtatcatgg cgactagcaa aacgatcgtg 79500ctgtacttgt gtcaggcgcc ggccacagcg tcgttgtacg ttagcgcaga cacggacgcc 79560gacgagccta ttatttattt cgaaaatatt acagaatgtc ttacggacga ccaatgcgac 79620aagtttactt attttgctga actcaaacag gagcaagcct tatttatgaa aaaagtatac 79680aaacacttgg tgcttaaaaa cgagggtgct tttaacaaac accacgtatt gttcgatgca 79740atgattatgt ataagacata tgtgcatttg gtcgacgagt ctgcgttcgg aagcaacgtt 79800atcaactatt gcgaacagtt tatcacggcc atttttgaaa tttttacgct cagcagtaaa 79860atcgtcgtgg ccgtgcccgt caattgggaa aacgataatt taagtgtact tttgaaacat 79920ttgcacaacc taaatctcat tggaattgaa attgtaaatt aaaacaaatc atgtggggaa 79980tcgtgttact tatcgttttg ctcatactgt tttatcttta ttggacgaat gcattaaatt 80040tcaattcctt aaccgagtcg tcgcccagtt tagggcagag cagcgactcg gtggaattag 80100acgagaacaa acaattaaac gtaaagctga ataacggccg ggtggccaac ttgcgcatcg 80160cacacggcga taataaattg agccaagtgt atattgccga aaaaccgcta tctatagacg 80220acatagtcaa agagggctcc aacaaggtgg gcactaacag cgtttttctg ggcaccgtat 80280acgactatgg aatcaaatca ccaaacgcgg ccagcacatc tagtaatgta accatgacgc 80340gcggcgccgc aaactttgat atcaaggaat tcaagtccat gtttatcgta ttcaagggtg 80400tgacgcccac taaaactgta gaggacaatg gcatgttgcg attcgaagtc gacaacatga 80460ttgtgtgttt gatcgacccc aacacggcgc cgctgtccga acgagaggtg cgcgaattgc 80520gcaaatctaa ttgcactttg gtgtacacaa gaaacgcggc agctcagcaa gttttattgg 80580aaaataactt taccgtcatt aatgctgaac aaaccgccta tctcaaaaac tataaatcat 80640acagagaaat gaattaataa aacaaaaagt ctatttatat aatatattat ttattaacat 80700acaaaatttg gtacactagt gttcaaatcg tttctgttca acgccattgt catgttataa 80760aacacatttg tagttttatt gtaattattt ttaaatttat ttttaatttg ctgtaataaa 80820acttgttcat taaatacaaa agactttgaa ctacttgcgt ttatattctt tttataattg 80880tactgaacaa acgaggggtg caaaaagttt ttgaaatgct gcacggcaat acctatcatc 80940tcctccattt tgtcctctcc tattgtaata gtggcactgc gcaccgtttt aatgtttaga 81000atgtaaatga gcgcatacag cggactattg ttggtgctca agcacattag gttgtgctta 81060tgcatagggt cgttgctcag cagcgttttg tatactacaa agcccgtttt ggggtcgcgt 81120ctgtacatta gtacgtgcga caaaaacaaa cgcaccggcg tcacaagcga ctcgtaatac 81180atgctttcta tcggaaactg tttggacttg atgtgttcgt acacggagcc ggcaaacttg 81240acgctgtcta caaacttatg gttcgtgtaa acaatcaaaa atctgtcttg tacaccgtcg 81300tcataatcgt ccacgtacag cggcttgttg ttaacaatta acattttgta gttggcttca 81360tactttagca gcccttggta ttttctgctc ttggaatcgc tcttgctcga atcggcatgc 81420ttcttaaagt acgactcgct gcattgtttc aactcgttga tagtgtacaa ctgcgagttg 81480agtttgctca cttccttgtc gctcgtttcc ttgttggact ctccgctgtg gttgtcatcg 81540tcaaacttgt gcatcaacac caaatagtcc aacagctcaa aaaacgacga cttgcccgaa 81600cccggttcgc cgggcatgta aatagccttc tttccgtaat ctacgggaat ggccaaacta 81660gcggcgaaat gcatcaacat aatcgcgttc gcgtgattaa aattggtgaa gcgtttaaag 81720tacaaatagc cttcgacaat ctttttcaaa taattgtacg agtactcctt caagtccact 81780ttggacatga tgatgcgcat gtagaatcga gtcagccaag tgggcaaatc gtccgtgctg 81840cgcgccaata tgattttgtc ccaccacaca ttgtacttct tcaagatcat taacgcgtcg 81900gcgtggtgcg tgtaaaattt ggaaatgtta tccgattctt caaactgaac atcgggttca 81960cgtgcaacat catcgcgcaa ttcggttaaa aacaaacgtt tatcattaaa cttgtccatc 82020aacatgtcga catattcgat tttgtgaatt gttcgataca agtactgaat aattttgttg 82080tgttctttgg aaaaaaactc tccgtgttgg ttaacaaatt cgctgttcgt gcgaatcaac 82140gtggtcgaca cgtacgtttt gttagtaaaa attagcatcc aaatcaattc gctcaattct 82200gcatcgttac cgaacatgtc cgccatcaag cagactttta gcgcttttct attgatcttt 82260attttcttgt agcatttgca ttttggtcga gatcccgata ccgttgaccg acacggtttg 82320cattttaggt tgtgcaacat gtcggaaacc ctgttcttgt ttacgtacag agcgagcgta 82380atcagatttt catcgtccaa attccacaaa tcgcgaaaca ggttgtttaa cgcgactcgc 82440atatcggctt ggcatgtgtt gcaattgccc atgtagttaa ctatggccgt gttagttttt 82500agcattttta catctcggca cattttggcg atgtgataag ttctataaat gctgagctcg 82560tcggcgctag tagatagcat gtaattaaac gcgtcctcgg gcaaatactt ttcgtcggtg 82620ggcttcttga atgtctgcgg caacgtggtg cccaacaaaa atggacagct cgaatgaaag 82680ctgttggtga acacgttgta cacaccgtgc gttgtcaagt acaagtattt ccaattgtta 82740aattttatgt tgctcaactt gtaacaattg cttttggtca atttgaatag gtcatcctct 82800ttctttacaa tttgataatg tttgccgttg aaaaccaaat tgactccggt cactacgttt 82860tccaattttc taaagaatcc tttacacaca atgtcaggcg gcaagtttag cgccatcaca 82920ttctcgtacg tgtacgccca caattcatcg tgatccaaaa tttcgttttt agccgactga 82980gtcaaatata tcatgtagtg tatgccaaaa taatagccca acgatacgca caatttggta 83040tcgtcaaagt caaaccaatg attgcaggcc ctattaaaca ctattttctc ttgttttttg 83100taaggctcac atcgcttcaa agcttcattc aaagcttctt tgtcgcaggc aaataatgat 83160tcacacaaaa gttccaaaaa cagtttgatg tcggtttctc tgtacgagaa attttcgttc 83220ttggtcaata tcttccacag tacatagatt aaaaaatcaa aatttttaaa tttgcttttt 83280tcaaagtatt gttgtagaag gtttggatcg ttggctcgtt cgtgggtcgc caaaacttta 83340accatgttct cgtgaattgc tataagcccc aaattgattt gcgtttgaat gtagtctgca 83400ttttcgctgc tcgccgatat aatgggtacg atgcgcggtt ttctggaacg cgtgtcgctc 83460aagtccacgt cgtttttgtc aaaattgttg ttctcgaaca ctctgaggct tttgaggttg 83520acgttgacga tatgcttgta cttgggcacc gtaatgcatt cctccaaatt aatgtcgtcc 83580ctaatgtaat tgaaaaaatt tttatccgaa ttgaccagct cgccattaac tttgcacgtg 83640gccacagtgc cgtcggccat tttgagtata aacaagtctt cgtgagaatc gtcaaacttg 83700gtttttccat ttacaaacag cgtttgcggc ggatcgtgat tcgtgcgcag gctgagctcg 83760acgttgagaa aacatttagg gtcaaacaca aacaaatcca cagggcctag ttttttgttg 83820tgtatgattg gtatcgtggg ttcgatgaca attccaaatt ttatatttaa aaacagctgc 83880catccgttaa aagagaaagc ttgctttttg ggccagttgg gccaataata gtaatcgccc 83940gcttgcacgc atttgttaat gtatccaggg tcggtgctct tgaaaaaatc ttcaaaatta 84000atatactttt gtatgatgtc atagtgcttc ttcaaaatga aaggttttac aaaaatgcaa 84060aaatcgttac tttccaacac ccagtcgtgg ccgtctaatg tttgagctgc gtgtttctct 84120gcaggttctt cggtgtcttc gcaagatgcg cccatgtcgt gtttcgcgca cggaccgtta 84180aagttgtttc taattgtgtt taagaactgt tgaaagttgt tgacgtactc aaacaatcta 84240cgtgttcctg ttcgcgtgtt tctaatgatt aaatgatttg catcttgcaa gttgttaatc 84300tcgtacgttt tgtcttgagg cacgtttttc aaaaaaaatt gtaaaatgtt gtcaatcatg 84360ttggctatcg tgtttgtact tttcgtgtta atttatttaa taatttcgat caaaaatcac 84420catccattct tacatagaat agaaacgcta atacaagatt tcaacaacac attgttgttt 84480ggcgcgtatg tacagattta cgatttaagc acgcccgccc gcaccgaacg attgtttatt 84540attgcgcccg aaaatgtggt gttgtataat tttaacaaaa cgctctatta ttacttggac 84600tcggcgaacg tgttttgtcc caacgagttt agcgtgacca cgttcacgca atccactatt 84660aaaacgatca acgagacggg aatatatgcc accgcatgca cgccggtcag cagcttgacg 84720ctaattgaac attttgcaac attaaaaaat aacgtgcccg atcacacgct cgttctcgat 84780gtggtcgacc aacagattca gttttcaata ctcgacatta tcaattattt gatttacaat 84840ggctacgtgg atttgttggc cgaataacgc gtatatagac gcttgtacgt tcatcgtagt 84900aatcatttta atacatttga ttgaactaaa catacatctg caatgggtga aagagtcact 84960aaattttgca atggaaaacg gcgataaaga agacagcgac aatgaataga gtttatattt 85020ttatttaata aaatattgtt cgtaatccat aatgttttgt attatttcat tgtgataatg 85080ttcccaatct tgcacggggg tggggcatcg tttgactttg acgtagaaat cgtacgcgta 85140gttattagtt ggcagatcgt cgacaagtgt gatcgacttg aaaaagttta catttttatc 85200gctcaaatat ttaattacaa tttttggcga tttgggtata ttgttgtcgg atcgatgatt 85260gtgaatgtca aaaacaaatt tattttcaat gaaacgcttt tttaaattgt aatctacaat 85320agcgttgtgt gaattttgaa ctaaatcaga gcgttcttct tgaacggtgg aaccttcgct 85380gataatgata tcaaaatagc cttccaaatc gacgtctcgc atcgagtgtg ctacatgatc 85440tctactgcca tacgaccaca agactaaaac gcaacccatc tcgtgcaact cctgcaagct 85500gtcatacaca aacggatctc gaatctcaac ttgctcctct tcggttatga gagtgctgtc 85560caaatcaaac acgaccacgt gcggaaatcc ccacgtcaaa gattcgcttt tgagagagac 85620cactttgtag tgtggcaata gaaaccattc tttaagaaac gaatacattg gcggtttgtt 85680gctaagcacg cacatgtggc ccaacactgg cgttttgaat gcgcgtttaa tattgtgcct 85740gatgtcgcgc atgtcgtcgg cgggcgcttt gaatatttgc atacagtaat tgtaattgtt 85800ttctatgatc ttgcacagct gcgggtcgtt gcaaaattga aatattacat attcaaaaaa 85860tttatacttt tcaaagccaa ggtatttgag gtcggcgtac tcgcttaaaa cgagaacatg 85920tcgtttgatg atggcgtcgt taaggcgcaa acagatccat ttgctttgaa gcgaggaggc 85980cataatgtac aaaaatggac cagttacgcc ttatttaaac tgtttaaaga gtttcgtata 86040aacaaaaact actctaaact aatagatttc ttaacagaaa attttcccaa caacgtcaaa 86100aacaaaacgt tcaacttttc gtctaccggc catctgtttc actcgttgca cgcgtacgtg 86160cccagcgtca gtgatttggt gaaagagcgc aaacaaattc gattgcagac agaatatttg 86220gcaaagctgt tcaacaacac aataaacgat ttcaaactgt acactgagct gtacgagttt 86280atcgaacgga ccgaaggcgt cgattgctgt tgtccgtgcc agctattgca caagagtcta 86340ctcaacacca aaaattacgt ggaaaactta aattgcaaac tgtttgacat aaagccgccc 86400aaatttaaaa aggaaccttt tgacaacatt ctttacaagt attccctaaa ttacaaaagt 86460ttgttgttga aaaaaaagga aaaacatacc agcactgggt gtacacgcaa aaagaaaatc 86520aaacacaggc aaatattgaa tgataaagtt atttatttac aaaacagtaa taaaaataaa 86580ctatttgagc ttagcgggct tagtttaaaa tcttgcagac atgattttgt aacagtcgaa 86640agccaaacga gggcaggcga cgaaatcgct tcgttcattc gctactgtcg gctgtgtgga 86700atgtctggtt gttaatagta gcgtgttctg taacttcggc gacctgtcga tgaacggctc 86760ctggatcttc tgtatgtgcg gggtctaccc gggcggcgtc tgtaacccga gcttctgcgc 86820ctgcgtgtcg aaccatatgt ggtaccggtt gaagaacggc gacggcgacg ataaaccatg 86880tttaaattgt gtaatttatg tagctgtaat ttttacctta ttaatatttt ttacgctttg 86940cattcgacga ctgaactccc aaatatatgt ttaactcgtc ttggtcgttt gaatttttgt 87000tgctgtgttt cctaatattt tccatcacct taaatatgtt attgtaatcc tcaatgttga 87060acttgcaatt ggacacggca tagttttcca tagtcgtgta aaacatggta ttggctgcat 87120tgtaatacat ccgactgagc gggtacggat ctatgtgttt gagcagcctg ttcaaaaact 87180ctgcatcgtc gcaaaacgga atttcggtac cgctgttgat gtattgttgc ggctgcaaca 87240tttgtatctt ttcgccgcgc tcgatcaaca attcttcaag agtggtgcgt ttgtcgcgct 87300gtaaagccac gttttgtaac agcactattt tcgcatatct cataatcgga ctgttgaaac 87360agcgtgcaaa cgacgaccgc ataatatcga cggtcgtcaa gtcgattgtg gtcgaaggca 87420tctccaacag agatcgcacg gcgtccaaca gcgtgtccgt ttgaacctgc gtcatttgcg 87480gtctgcacgt gtagtcgtca aacgtggttt cgagcagttt gaacaacgaa tgatactttt 87540ccgatcgcag caaaaatatc atggtcatga ccacgtcgct gattttgtat tctgtagaac 87600tggtgctgtt caacgaatag tgatggatta gtttgcgagc agcatttctg tatcggcgca 87660tgttgatcaa ctcttcggaa ggctgcgcgg gcgcggcggc gttggctcgc gcaaacaaat 87720ttattacggg acgcggcgta ggctgcgcgg acgctggcgc ggcgacgacg tccgcgtttc 87780ccgccgcgta ctgagacgct atggcagcgt tgttatttaa aattgtgttt tgcgatttgc 87840gagccacgtg catcataaaa tttatcaaca cgtcggtgtt caactgcacg ctttgatgtt 87900cgtcgcagag caaaggaaat agctggggcc atatcgccaa ttgcataggc tcgtctattt 87960ttaaccgcaa tttgtttatt tccaaataca acgcgatagc gctcatcgtg accgacgacg 88020cacacttact ctgtaactat cacttggatc gtgttgtcgt aaacgcttcc caaaaagtct 88080aacacgttga ccgtttcgat tctattcaac ttaattgtgg acgcgttggc ttgcatcggt 88140tccaacagac tgcgcgctcc gacagattga gtagacaaaa tttttaaact ttccgtctta 88200ttgggcgtaa tgtcgttgat taacaacgac gcagccgttt gagaggccgc agtgttgatg 88260gtttgcaaca tgtcgacggc cgccatttgc gtttgcgccg aaggtcttgc tggcggcctg 88320ttgcggcggt ttcttcgtgc ttgcgacatg ttgtcgtcag tgtccatatc ggtatcattt 88380attgaagcaa tcatggttga gttcgataag cagagatatt tcgttgtcca attggtactt 88440ggtaatgatg tgccttataa atgtttcggg cacaatcatt tctgtcatta gcacgttaca 88500aatatctatt ttgatcaatt tcaatttatg aattaacaga ttaatgtttt cgtccgagta 88560cttgctcatg atgaaacgac aaacgttgcg gagttccaac tccgctaccg gatacgcttt 88620gttgggcaaa ctctctaaat agtgtctcaa ataaaagccg atcaatacgg tggacgctat 88680tttgttaacc tttttcattt tagtattgcg gcccatttct atcatgaagt ttttaaacgg 88740tagcaacagc ctgtctccgt tagcaacagt ggagcagccg ttgcattgcg cgctcaaaat 88800actcaacacg cgctcgtgat cttcttggcg caatccgacg gttgcttttt tgcattcttt 88860gacaaatggc acgcacatgt cgcgtttcgt gtacaaagaa tacgctttgt cgcaaatcaa 88920gttatagaaa aattgcacaa atatctgcgt aatcaagttg ttttcgttaa taatgtcact 88980ttcgtttttg taatcggttc gaagcaacac gtacaacatc agaggcatgc cgaacatggg 89040tcttaaaaaa atgtcccaac cattttgcaa gcccgcgtcg agggtgctca gcgaggacgc 89100caagtatttg catttgcact caaaacattg aattttgttt gcgggcttgc acgactgaca 89160catgatcgca tccacgtcgg gtgccggcgt cggattgtaa tatttttgca agtattgcat 89220aatggtccta aaatggggta cctgtttgat aaactcgtcg cgcaaaaata tcgaaaaaat 89280gttttttaca ttgtgtatgt tgtctgtgtt gttggcttga ttctcaaaac tactctttat 89340ggaaacaata catttgttaa attctgtgaa aaaagtaaga cctttactgt ccacgatcaa 89400gctttggttg aaatattttg aaaataaaaa acacaacgaa tcgatttcat cttgtaacaa 89460ttgcgcttca aaacacacgt tttcaaagcg gtcgtaaatg ttaaacctta aactgtattg 89520taatctgtaa gcgcacatgg tgcattcgat ataaccttat aatatgaacg attccaattc 89580tctgttgatt acgcgtttgg cagcgcaaat actgtccaga aacatgcaaa cggtggatgt 89640gattgttgac gacaaaacgc tcagtttgga agaaaaaata gacacgttga ccagcatggt 89700gttggctgta aatagcccgc cgcaatcgcc gccgcgggta acatccagcg acctggccgc 89760atcgatcatt aaaaataaca gcaaaatggt gggcaacgat tttgaaatgc gatacaacgt 89820gttgcgtatg gccgtcgttt ttgttaagca ttatcccaag tattacaacg agacgaccgc 89880cggtttagtt gccgaaatag aaagtaatct gttgcaatat caaaattatg taaaccaagg 89940caattatcag aacattgagg gttacgatag tttattaaat aaggcggaag agtgttatgt 90000taaaattgat agactattta aagagagcat taaaaaaatc atggacgaca cggaagcgtt 90060cgaaagagaa caggaagcgg agagattgag ggccgaacaa actgccgcaa acgctcttct 90120ggagaggcga gcgcagacgt ccgcagacga tgtcgttaat cgtgccgacg ccaatattcc 90180cacggcattt agcgatccgc ttccaggccc cagcgcgccg cggtacatgt acgaaagttc 90240agagtcggac acgtacatgg aaaccgcccg acgtaccgcc gaacattaca ccgatcagga 90300caaagactac

aacgcggcgt acactgccga cgagtacaat tccctggtca agacggttct 90360tttgcgttta atcgaaaagg cgctggccac tctaaaaaat cggttgcaca taacaactat 90420tgatcaattg aaaaagttta gagattatct gaatagcgat gctgatgctg gagaatttca 90480aatattttta aaccaggaag attgtgtgat actgaaaaat ttgtcaaatt tagcgtcaaa 90540gtttttcaac gttcgttgcg tggccgacac gttagaggta atgttggaag cgcttcgcaa 90600taatattgag ttggtgcagc ctgaaagcga tgccgtacgg cgaatagtca taaaaatgac 90660gcaagaaatt aaagattcga gcacgccgct gtacaacatt gccatgtaca aaagcgatta 90720tgacgccata aaaaacaaaa acattaaaac cttgttcgac ttgtacaacg acaggctgcc 90780aatcaatttc ttggacacgt ccgcaaccag tccagttcgc aaaacttccg gcaagagatc 90840tgcggaagac gacttgttgc cgactcgcag cagcaaacgt gccaatagac ccgaaattaa 90900tgtaatatcg tcagaagacg agcaggaaga tgatgacgtt gaagatgtcg actacgaaaa 90960agaaagtaaa cgcagaaaat tagaagacga agattttctc aaattaaaag cattagaatt 91020tagcaaggac attgtcaacg aaaagcttca aaaaattatt gtggtcaccg acggtatgaa 91080acggctgtac gaatactgca actgcaaaaa ttctttagag actttaccga gcgccgctaa 91140ctatggcagc ttgctcaaaa ggctaaacct gtacaatctc gatcatatcg aaatgaatgt 91200aaatttttac gagttgctgt ttccattgac actgtacaat gacaatgata acagtgacaa 91260aacgctttct catcaattgg taaattacat atttttggcc agtaactatt ttcaaaactg 91320cgctaaaaac ttcaactata tgcgcgaaac ttttaacgtg tttggcccgt ttaaacaaat 91380cgactttatg gtcatgtttg ttataaaatt taacttttta tgcgacatgc gtaattttgc 91440caaattaatc gacgagctgg tgcccaacaa acagcccaac atgagaattc acagcgtgtt 91500ggtcatgcgg gataaaattg ttaaactagc ttttagtaat ttacaatttc aaaccttttc 91560aaagaaagac aagtcgcgca acacaaaaca tttgcaaaga ctaataatgt tgatgaacgc 91620aaactacaat gttatataat aaaaaattat aaaatatttt taatttttat ttatattcag 91680tacatttaca catattaaca tattgtttat acaaattctt ataatcatta tgatttaaat 91740tgaattgttg tctaaacaaa ttaaacactt tattaaacaa taacttttcg ttgtaatttt 91800ttactttgca catgttataa caaaaaatta aaattttcat catgtctgat ttgtctatgg 91860cgtcacagtt gcttttaatg taatcgcaag ttaaccactc aaaaggaccc ttttctattt 91920ttaatttgtt taaatcttta taatcagact tcagtttgta aattagattt ccacatcgaa 91980taataaatcc ttccagcggg ctttggggaa acattaaaga cttgaaattt aacctttcta 92040caaaatcgtt gtacaaatat ttgtgacacg gaatagtatt aaaccccacg ttagtcaaca 92100actcttgcgc ctccacaaag ggcacaaact ccccgccgta taattgaatt tcgtaagcgt 92160agtatttcaa actctctttc tggtccacgt agttaattac gttaatgggt gtcgtttttg 92220cgtcgtcttt ccaacccatt aattcgccgt agacaataaa accgtcattg aaccgcgcct 92280gaagcgatcg catgcacgtt tctaaatctt ttcgaatgcg gtaataattc ataaaattgc 92340cgtccggtct gtaagtgttt cttgacccgt acgtaatttt attttggttg caaatgattc 92400tgaaattaca accgtccaac ttttcttgaa caataatttc tttgtcggcc aacgtacctt 92460ttttaccttg atctagatgc gacacagatg gataaatttg atacacaatt ttattctcat 92520cttcgggcat tacgggtccg cgttcattta acgcgtacat gacaatgttg tggcgaatgt 92580cggtgcgctc cggcggttct ggcacgtggt gcagtctgtc ctgcaattgt tgcttccatt 92640gttgaaaata ttcggtccat tcttgttgat actcgccgcg ttgcatgagt tttacgtaca 92700gttttaaaag tttgacattc tttacaaata acgttagagt ttcgtcgatt ttgtatcctc 92760cattattttt gtttaaatcc aatacattta aatcgttcac taccagttga ttgtttttat 92820ccatcgtaat ttttatctca tcgcccacgt tgaacaacat gtttaaaatt ttggtggatt 92880tcggcgcacg tttataatct aaataatatt caacgtacac gtaattgaac atgagctgca 92940acaatccttt ggcattgttc aaaattttgt atctcatcaa agtataaata attttcacca 93000tcgacaccgt catcaacttg gttacaaact cgtacaattg caagttttca ataccgtatt 93060tgtctttaaa atcttcacgt ttactgaaca tgcttaattc gggagatttt ccagtcaaaa 93120tgccaattaa tcccgtgtac aagtcaacgt atttgacatc gttgcccgat tcatcttttg 93180catgtcgatt tttcaaaagc tctttattgt cgataaattt ttcaaaggtc tctcgatcac 93240atttagtgta aatatggtag tcagtgtcgc tgctttcgac cgcgtatccc ttggcatggc 93300tgcccgtatc aatgcaaatg tacaccatgt tagaatgtgc tgcttactgt gcctgtatca 93360agccttatat acctcaaaat atttcacatt tttgcatcat cgtaaaatat acatgcatat 93420aattgtgtac aaaatatgac tcattaatcg atcgtgcgtt acaagtagaa ttctactggt 93480aaagcaagtt cggttgtgag ccgtgtgcaa aacatgacat cataactaat catgtttata 93540atcatgtgca aaatatgaca tcatccgacg attgtgtttt acaagtagaa ttctactcgt 93600aaagcgagtt taaaaatttt gtgacgtcaa tgaaacaacg tgtaatattt tttacaatat 93660ttaagtgaaa cattatgact tccaataatt ttgtggatgt ggatacgttt gcaagacaat 93720tgattacaga taaatgtagt gctctaatca aagtgcggat ctgttgccgg caaacatttt 93780agagattgta gagaaggcca gagacaagta ttttgagggc caactcaaaa aaactatgaa 93840tacattaaaa aattattttt acgaaaaaat atatggacga ttcgatagat tataaagatt 93900ttaacagacg catcctattg atagttttta aattcgcttt aaacaagagc acaatacttt 93960ccatcgtaca aagagatcat cgagtggcca ttaaacgttt aaacaaaatt aaccccgatt 94020taaagagttc tccgcgcaat gcttcagcat tacaatgaat gtttggaaaa tctagacaat 94080ccagtcacgg acgaacatca tttgttgaca aaagagttgc tacaaaaata tttatcgaag 94140cgtttgaata cagttacacc aacactaatg ccatcagcat ggacaaaaca gatgaatttg 94200attttattaa accggcattg aaacctttgc cagatgcaag accgccatcg cttttggcca 94260acgtgatgaa cgaacgtaaa agaaaattac aaaacaccaa ctcaacggca aaatgtttgc 94320taccagcacc accgccacaa ttgcgtaaac ttgaaaaaaa gaatcattta ttgcctttgt 94380tttctttgta attatattgt tgcatttcta tttctaatat catagttttc taataaagta 94440gtttcatatt tttgtttttg tacagtaatt gtttcttggt ttaacaagat cacaaccaat 94500aacataaaga ataacacaat cataacaaaa attaaaaagc cgcatactac tagaacaaat 94560tctttaatta gcgatcggtt tctatttaca aattggccga gctgatcgcc ttcagtcggc 94620gagttgtggg cttggatgat gtcgacgata ttgttgccgg cgcgaccgcc tgtcgctctc 94680gatataatgt cggccgccgt cggtttcatg atgtgcttaa ctacaaataa tagttgtact 94740tgacgggcgt caccgtgatg ccgctgctaa aacctccgtc cgttaagacg cgttgcgtta 94800caaaattaat gtttgtccga ttagcgtagt cggaataatc aaacgtgttg ggcggactaa 94860aatcgggcat gttgatgggc acaatgccgc tggagctgat agcaatgctg tcgttcttgc 94920aaaacagccg aatttttttg tagggctctg ctttattcgg cgcagacgac accatctggt 94980caaagttgtt caattttatg attacgttgg gtaccaattg ataggggaaa attattttct 95040ggaacatttt gacaaagtcc acaaccgttt ggctatagtc gggaatgccg agcaaagact 95100gcgcctgttt aatgtatttg agactggagc ggtttactgt agcgcaattg gatggcacgt 95160cgcccttcat aagccggcgc gttctctccc aattcaattt gttgtacaaa ttatcaatct 95220cctcgtgcgg cagattgatt acatagcgcg cgggctgttt gcgatattga aagatgcaaa 95280aaatgcgttt caacgacaat atcttcacca tggtggacgt ttccagattg aaacataaca 95340aaaagtcatt gctttccacc aattctttaa aatgagacag cggaatttca caagcgatcg 95400gtcgcaaatt gctttttatt ggaggcggaa cgctttgacc gttgcggttt tttagtaacg 95460cgctgcacgc agattgcatg tccgtttcgg gatacgtaaa ctcgatggga catttggggt 95520tttcatggtg aacgatcata gtgttgcaat aaaacaagtt gttggtcagg agcacgctaa 95580aaacacgcgt ttcgcccgca ccgatttcgg tgatgggtac caacgggttc cagtagacta 95640tggtggcgga cgctgttttt tttggcgatc gactgtctat gttaacatca tgctcgtgcc 95700tgtacactag cacagaattg aattttggaa attgtttttt gtcaatgtac aaccggtcgt 95760cgtctgtggg cacgtacacg atcaagtttt cgattaattt gttgcctacg tcgctttgcg 95820gttccaccaa attgtgaggg aacgcaaaaa agcgatcgct aatacaaact tgaatctgaa 95880acgggcactc catcgtgatg tatatgtctt acttcattag actttagatt attttaattt 95940gtgaactcgt accgtattca atagggtgtc gggcacgtaa ttgtaatggt aaaacagatc 96000ctgttgaaca cgtgcgttgt tcactacgat tgaaatgcaa aaatacatca agtacataaa 96060cactatgatt agaaaggtag cagacagaaa atatttcatc tttaaatctt atgctagttg 96120aataaaatac atagtacttt tatacgttta tttatatttg ttttctttgt tataaccgta 96180attgtaaaac ttgtgatcgt gctcgccagg cataatttct ttgcacatca gcttgcgaat 96240atatgtgaca tcttcgtaca ccgatttctt gatgttacca tcgtgaagcg ttgtcggctt 96300gagaggtttg cggtcgttgt tgtaaaaatt ttgcaccgaa taattatcca tagtgcagca 96360caggcaatgt cactgatgca tatgctttaa ttttttattg cattcagtta ttatatgatt 96420taataaacgt acacaatagc acgtttatcg gttaaagata actttcaata tataaaagtg 96480tttgaattgc gagaccgtca acataacgtt tatcaacgcg atgactaaac gacaatttgc 96540tttgctgttt gtgtggcacc acgacaacca atttgtttgc aacacggacg aatacccgtt 96600ttggcacaac attgaatacc atgcacggcg ctataaatgc atcgttttgt actgtgtgga 96660aaacgacgga tcgctacaac tgcccgtttg caaaaacata aatctcataa attataaaaa 96720agcgtatcct cattattatg gaaactgtgt tgacagtata gtgaaacgtg ctggcaaaaa 96780ttgattatat gaaagtaact gcaatgttaa acccccacct gttggacgtc gcgtacaatt 96840atttgctgtt gatggacatg gattgtgtgg tgcaaagcgt gcaatggaaa caattgtcaa 96900ccgacacgta ttgttttgag ccgttttacg actctcaaat taaatggttg tacgcgccca 96960aaagcggaca aagttttgat agttatcttg aaaactatgc aactctaatt cgagtcaaac 97020aagtgcagca acatcgaaaa gaattaatac tgcattgtgt ggattttctt acaatgaaag 97080caaatgacaa ttttatggtg ttcaaaaatt atattaacat gattataaaa gtgtatttgc 97140aattttacaa ttacagattt cccatcaatt ttgaggacaa cacgatgaaa ccttgtgtaa 97200atttaacttt tagacgtggc ggcagttgga aaactcaact gcaacccgta tgcaattatg 97260tttacaaaag taaaaatatg ccaaaattta ttaaataaaa caaattaatt taaacaagcg 97320tttttattga caatactcac atttgatatt atttataatc aagaaatgat gtcatttgtt 97380ttcaaaattg aactggcttt acgagtagaa ttttacttgt aaaacacaat caagaaatga 97440tgtcattttt gtacgtgatt ataaacatgt ttaaacatgg tacattgaac ttaatttttg 97500caagttgata aacatgatta atgtacgact catttgtttg tgcaagttga taaacgtgat 97560taatatatga ctcatatgtt tgtgcaaaaa tgatgtcatc gtacaaactc gctttacgag 97620tagaattcta cttgtaacgc atgatcaagg gatgatgtca tttgtttttt taaaattcaa 97680ctcgctttac gagtagaatt ctacttgtaa aacacaatcg agggatgatg tcatttgtag 97740aatgatgtca tttgtttttc aaaaccgaac tcgctttacg agtagaattc tacttgtaac 97800gcaagatcgg tggatgatgt cattttaaaa atgatgtcat cgtacaaact cgctttacga 97860gtagaattct acgtgtaaaa cacgattaca gcacttcgta gttgtatcga aaattgttca 97920atggctcttt gttaatgtcg taattgatta atatgtcgta caatttggcg gcgttgtgtt 97980tgcacacgac cgtttttagt tcttgaaaca ttttttcgtg tatgtttagc atgttgtatt 98040tcagagtgcg atgtgtaatg ctggtgacga gcatcaaaat gataaaatct aaagcggcta 98100atttgtaatc ccgttcatac gctctgtaat cgccaacaac tctgtggcca gatcttttta 98160gattttgaca ggcgttatgg tacgaattga taatatttac tatagtttct cttgttatcg 98220gtttgtcgat taaactgtta acaaacatca cgttgcccaa gcgcgacggt ttagacaccg 98280acttgttttt tgtctgttca aatttgtaca aattaaaaac gctcatagac tggtcgtcag 98340gcagtgtgtc gttatacaaa caaaatggta aaacgtttaa ttcgacaaac gacgagcaca 98400ttaaagtttg ttggctgtta acgtcctggg gatgtaaact gttattcata acgtaacaca 98460cttcaatgtc ggaatgcttg ttttcaaatt tgtccttgtc tacagtttca atggtgattg 98520agcgaggttt gagtttattt tctaaattca tttggatatt ttcaatatgg tataccaccg 98580acacgttgtg agccagcgat ccttgattgg ttttaatcat attcaaaata ttcatgatat 98640ggttgaaaaa agagtctgtc aaaacgtttg tgtcgttgtt aaatatcgct ttccagggtt 98700tactgttgcg tgactcaacg acggccgtgt aacataacaa gcgcgccagt tgcatgtgcg 98760acaacttaat gttatcaatg tcggtgatgt ttggcaccag attttcattg ccgtcttcca 98820gtagcgtgct cagttcggtc gagtagttat tcaacgatcg attgtgcgat tcaaacaagt 98880ttactatcgc aggttgtaca tagtttttta tgtcgtcaaa ttgaattata tcgatcttgt 98940ccttgttctc cagcataaac gacaaatttt ttaggtcgaa tttaatattt ggcgcgtttt 99000cgttggactt tttgtaattt aacaacatcg ccaacagttt gtgtaactcg ccgttagctt 99060gatctttgct aaacagttta ttggtagcgt aattcacgtt gtcgttcaaa aacagcaact 99120cgttgatgat cattttttgt aaaagcgcgt acttgctcat gttgacagaa tctcttacat 99180ttcagttgta aacgcgtctg tacaaattgg ccatgcgatt cggaatgcac acggggatcg 99240tgcgagccag tgccgtttgg cgaaatagca ttttttcata gccgctcgaa caatcgcacg 99300cgtccggcga aaattgcacc gtgttcaaat tcatattcaa ccggccgtcg ttgcatagat 99360aaggcctcgg tgttcccgta tcgtccacca agtctctgta cgtgctcacg catgtttgag 99420acacgacaaa atctccgccg gcggagaaaa cgtgaaccaa gcccagtgcg ggatcgcatt 99480ctatcaagtc cggagcctgc gcgtttacca aagcgtcgga ggcgttgcaa aagccatcct 99540ggcaggtcaa ctcgtttgca gcgctggaga tcacgcagtt gtctctacac tgctgatccg 99600tcacgcacgg taaccggttc aatgaacaat ctacgcctcg attgcgctga aacgtaaaat 99660ttaacggcgg cgcttccaac tcgttaatgt gcatgtatgc atcttgcaaa ataaattttt 99720gaacaaattt aaacgtgtac atgtacacga ttagtataat taccagtaga ataagtattt 99780gccaaaagtt caacatgatc gtcttaactg agtgtgaaaa gcgtggtgtg acgcacgaaa 99840tgactggttg cgcaaaaaat aaaccggggt ctatataact cggcgtcgac cgcgttcatt 99900tttaccgtca tgcatctgac ggctaatgta ttgctcgttc ctaacgcgct caaaaagcgg 99960gacgtgaaat acatttataa tacctatttg aaaaattaca gtgtaattga aggtgtgatg 100020tgttgcaatg gcgattgttt ggccgtggtg gtgttggacc gaaatcagct gcaaaacacg 100080gacatggaag tgttggagag tttagaatac actagtgaca acattgaact gttatgcgaa 100140aaaatatgtg tgatagttga taattacgac aagtattacc aaaaaaattg tgtataaata 100200aaataccaaa ttttattata tcattttgtt ttatttaata attaaagaat acaacgccac 100260atctattcct agtacaacaa ataatttgat tattattttt gagtgcacat taaaaaataa 100320caaacagtgt aaaaatacta cagaataata caatacataa atattatagt aaatagctgc 100380aattttgata gcgtaattta tactttgata tttttcaacg tacaacgtta aatgttgata 100440cgcattattc acaaataaca aaatttttct aatatgccat ttgtccgcaa ttgtttttgc 100500gatatcaaag cctttttcaa acaattgaaa aattgcaaac aaaaccacgt acatgacgtt 100560atacatagtg ttaaagtttt tacataacaa ttctataatg aagaaaattg ctaaacacgg 100620catgagcgcg cacataatcg cgttggccgc aaatatctcg tacgtacaaa aatactcgga 100680cattctccaa taagtaaaat gcattttgct attatactgt tgtttcttct agtgattatt 100740gcaatagtgt acacgtatgt agacttgata gatgtgcacc atgaagaggt gcgttatcct 100800attacggttt ttgacaacac acgcgcgccg cttattgaac cgccgtccga aatagtaatc 100860gaaggcaatg cacacgaatg tcacaaaact ttgacgccgt gcttcacaca cggcgattgc 100920gatctgtgcc gcgaaggatt agccaactgc cagttgtttg acgaagatac aatagtcaag 100980atgcgtggag atgacggcca agaacacgag acgcttattc gagcgggaga agcgtactgc 101040ttggctttgg atcgagaacg cgcccgatcg tgtaacccca acacgggtgt gtggttgttg 101100gccgaaactg aaactggttt cgctcttttg tgcaactgct tacggcccgg acttgttacg 101160cagctcaaca tgtacgaaga ctgcaacgtg cccgtgggct gcgcgcctca cggccgtatc 101220gacaatatca acagcgcttc gatccggtgc gtgtgcgacg acgggtacgt gagcgactat 101280aacgccgaca ccgaaactcc gtattgccgt ccgcgcaccg tgcgcgacgt aatgtacgac 101340gagagttttt ttccgcgggc gccatgcgca gacggccaag ttcgtctgga tcatccggcg 101400ctcaatgatt tttaccgcag acactttaga ctcgaagaca tttgcgtgat cgacccttgc 101460tcggtggacc cgattagcgg gcaacgcaca tcgggacgct tatttcacca accaaccgta 101520aatggtgtgg gaatcaacgg atgcaattgt ccggccgatg acgggttact gcccgtgttt 101580aatcgacaca ccgccgacac gggcatggtt agacaaagcg accgcaccgt cgcgaacgct 101640tgcttgcagc cgtttaacgt gcacatgtta tcgttgcgtc atgtggatta caaatttttc 101700tggggccgca gcgaccacac cgagtttgcc gacgcggaca tggtgtttca agcgaatgtc 101760aaccaactca gtcacgaacg gtatcgagcg attttgtact cgttgctcga gtcgcacccg 101820gacgtaacag aaatcgtaac agtcaacatg ggtgtcatga aaatttccgt gtcatacgat 101880accacattga aaaatatact attaccatct tctgttttta ggctatttag atttaaagaa 101940agtggcactg ctcagccggt atgcttcttt ccaggcgtag gacggtgcat aaccgtcaat 102000tccgattcgt gcatcaggcg acacgctggt ggtcaagtgt ggaccgcaga aacgttcacc 102060aactcgtggt gtgtactgag tcgtgaaggt acgcatataa aagtttggag tcgcgcgtca 102120cgatatccac gcggagacgc gcctgcagcg ttaagattgc gcggcttctt tctgaacaac 102180gatcgcgaac gaaacacaat aagagcggtc actacaggcg acatgaccca agggcaacaa 102240atagacgcat taacccaaat acttgaaact taccccaact actctgtata acaacatgag 102300cattttaaaa gttgtagaag cgtgcaattt ggcacacact tttttaaaat tgggttattt 102360atttagggcc aagacttgtt tggatatcgc tttagataat ttggaactat tgcgtcgaaa 102420gactaacata aaagaagtgg cagtcatgtt aaacaagaaa actacagagt gtttgcaatt 102480gaaacgaaaa atagataaaa aaattgcaca acgtgtttta ataaaaattt acactatcaa 102540atgatgacat cataacgggt tcaatattct gtgtgcaaaa ataaatgaca tcatatttca 102600aacttgtttt acgcgtaaaa ttctactggt aaaacaagtt tgagatatga tgtcatcatc 102660acaaataata gtatgtaata aaataaacat atttgtgtgt aaatataatt tattacaaat 102720aaattttaca ttgaatcaat ctgtcttcgt gtttgttgta aggtcttcga atcttgtgtt 102780tcagcccctc gggatggtca aaatgcgccg tagtaattgt taatggatct ttcaacgatt 102840ttttgcccat ggcgagtgtg acaaacgcgg ccacgacaaa cagcaggata atcagtttca 102900tggtgttcta tattcgacaa tatatgggtc gcttctaaat caccttgtcc ccaaaagcct 102960cttttatagt tttttagaac acgttgtgta ttccaacagt aattgttcca tctctttcaa 103020cagccattca gcatccggtc gttgactgta atcatgctga attaatttac aaacaatttc 103080ggtcaattta ggatggcctt gggataaact tgccggcatt tgctgtacat tgtttctaaa 103140gttagttagc gtagtttcgc gttccaaagc agtcttgaag ggcattatca attcgaataa 103200aacaatgccc aaactataca tgtcattttt gggggtgtac acttttttga tttgttctgg 103260tgcagcgtac aaagttatat tttgagggtt gtttttgata aacgttttgt atagactgcc 103320aaacatgccg cccacataca aatcaaagtc gggcccagtc atgaaaatat cttcgggatt 103380aatattgtgg tgcacgatat ttacggaatg aatcgctttc acggcgctca ccaaatcaac 103440aaacttgcta atataaaagc caaaatccgc cggaacttta atgttggtct ttgcaaaagt 103500ttgcaaattg cgttgtttca aatagtcgct caacatgtac tcgtttagag gcgacgcaat 103560atatatgcgg tgctgccgcg gattcaaata aaccaattgt tcgggtttca tggtatacag 103620ttaagtgtta acgcgtcact aaattcagac acgagcgcac gccctatata catacaattt 103680atcgcacaag atgcttaacg cgatctgttt ataaactaaa acgcactgca ataaatttta 103740gcaagcattt gtatttaatc aatcgaaccg tgcactgata taagaattaa aaatgggttt 103800gtttgcgtgt tgcacaaaat acacaaggct gtcgaccgac acaaaaatga agtttcccta 103860tgttgcgttg tcgtacatca acgtgacgct gtgcacctac accgccatgt tggtgggata 103920catggtaaca ttcaatgact ccagcgaatt gaaatattta caatactggt tgctgttgtc 103980gtttttgatg tccgtggtgc taaacgctcc gactctgtgg acgatgctca aaaccacaga 104040agcccatgaa gtaatttacg aaatgaagct gttccacgcc atgtacttta gtaacgtgct 104100gttgaattat gtggtgtttt tggacaatca aatgggtaca aattttgttt ttgttaacaa 104160tttaattcac tgttgtgtac tttttatgat atttgttgaa ttgcttatcc tgttgggcca 104220cacaatgggc acgtacacgg attatcaata tgtcaaatcg tgttatatgg ttatattgtt 104280tgtttcagtt atgagtgtta ctattgttat gggtttagag tgtttgaaaa cgaaactaat 104340tgataacagt ttgatgttta acgcgtttgt gtgcgctttg tacattgtga ttgcaataat 104400gtggtcttta aaaaataatt tgactagtta ttacgtttca aatttacaaa gtattcaagt 104460tgttccgttt tcatacaacg atccgccgcc accgttctct aacattgtaa tggatgacat 104520aaaaaataaa aaataattta taaaaatgtt ttttattctt tcacaattct gtaaattcta 104580aacaaaaaat ataaatacaa acttattatg ttgtcgtcta aataaacatc aatttgtaaa 104640tctggacacc tattcatatc attgatatta cagtctacta tacaacaatt aaaactaacc 104700aaattatctt tacaacaatt aaagcaatta aaacaattta aataatcttc attgtcgtcg 104760tataagttta tttgcactgt agacggtgtt acacagcgat ccattcgacg ttcgtgttcg 104820atcaactttc tcgccaactt gtaccataaa aattgtttgg acaaaaagtt ttccaacaat 104880ggtaacggcc aattcaacgt gacgatgcgc acgtcctcgg gtatgcattt gttaaaaaac 104940acacagctcg ctttaccaaa cgaaagcaaa ggtactaaat atggcgccat tggctgattt 105000gttattccaa gataattaca aataaactga tccgtcgtgg ggtgataact ggcaggtgtc 105060agctttaaat aatcttcaac gttgttgtcg cgcaaaagtc tgcattttac acgcgttgtt 105120aatcccacga cttttgcatg taaaatcgga tccaaatact gcagaatcgt gtctataatt 105180tctaatggta aacgtatgcg ttttgctcgt gggcgctttg taacgctcga catcctaata 105240acaactaaca caaaactaaa atgatactca atatattgct tttacagttc atctttaggt 105300ttaaactgtg cgtttatcgc gttgagcaag tcgccgttat cggcatcaat ctcccaagca 105360aacaggccgc

ccaatttatt tcggtcgaca tatttaactt ttcctaacac agagtcgacg 105420ctgtcaaacg aaatcaaatc acctttactt ttatcgaaaa cgtacgacgc ttgagcggcg 105480ctgtcaaacg tgtacacata attgttgaga tctttttgaa tttgacgata atctacaaca 105540ccgtcctccc acgtgcccga ccccggcccg ttgccagtgc cggaaaaata gttgtcattc 105600gtataatttg ttacgccggt ccagccgcgg ccgtacatgg cgacgcccac aattattttg 105660ttgggatcga cgccttgttt cagtaacgca tcgacagcgt agtgtgtagt gtatagctct 105720tccgagttcc aacttggcgc gtagactgtt gtttggtagc ccaaatccgt gtttgaccaa 105780gcccctttaa aatcgtaact catgagaaat attttgccta atgacttttg cgcttcggcg 105840tagtttacca cggcaatctt gtcgtaaccc gcgcttatag cgcttgttaa ttcgtaaacc 105900ctgccggttt gcgcttcgag gtcgtctagc attgcgcgca gctcctccaa caacaaaatg 105960tatgttttgg cgtcaccgtc cgcatcgccc aacgacgggt tagccccttt gccgcccgga 106020aactcccaat cgatgtctac accgtcaaag aatttccaca cttgcagaaa ttccttaacc 106080gaatctacaa aaacgtttct tttttcaaca tcgtgcataa aataaaatgg gtctgataga 106140gtccagcctc ctattgaagg aagaattttt aaatgggggt ttgctaattt tgccgccatc 106200aactgtccaa aattgccttt atacggctcg ttccaagcgg acacaccttt ttggggtttt 106260tgtacggcgg cccacggatc gtgaatggca actttgaaat cttcgcgtcc cttgcacgat 106320ctttgcaaag attcaaagct tccgggtatc gttttgaggg cgtcgtttat tccatcgccg 106380ccgcagatgg gtatgaaacc atacaacaag tgtgataaat ttggcaaggg aactttgtct 106440acgggaaagt tgcgcccgta cacaccccac tcaacaaagt acgcagcgac aattttatcc 106500tctctcctgc caggtttgtt gttttccagc catgtgtatt cgagcggtgc cagatggccg 106560ccgtcggtgt ctgcgacttt gaccaacacg ggatcgctca cggaacagcc gtcctcattg 106620caaagtttga cacgcatgtt aaattgcccg ctcacaagaa ctttaatggt agccctttta 106680ctttcggcgt cgcctttcca tacctgctgc tcgtcaaaca acacgtacgc tatgtcgcca 106740atgtcgccgt tccagacgtt ccaactgact tgaacgtcga cttgttcttt aggctttatt 106800aaattttcgt aagcggtggc ctcgtaattt atttctacga gcgcataatt gcgatcggcc 106860caatcgatca ccggcgtgcc gggaatcgcg ttagaaacgg cgaccaacca caaaacgttt 106920aacaatttgt acaacatttt aatttatctt aattttaagt tgtaattatt ttatgtaaaa 106980aaatgaacaa aattttgttt tatttgtttg tgtacggcgt tgtaaacagc gcggcgtacg 107040accttttgaa agcgcctaat tattttgaag aatttgttca tcgattcaac aaagattatg 107100gtagcgaagt tgaaaaattg cgaagattca aaattttcca acacaattta aatgaaatta 107160ttaataaaaa ccaaaacgat tcggccaaat atgaaataaa caaattctcg gatttgtcca 107220aagacgaaac tatcgcaaaa tacacaggtt tgtctttgcc tattcagact caaaattttt 107280gcaaagtaat agtcctagac cagccaccgg gcaaagggcc ccttgaattc gactggcgtc 107340gtctcaacaa agtcactagc gtaaaaaatc agggcatgtg tggcgcctgc tgggcgtttg 107400ccactctggc tagtttggaa agtcaatttg caatcaaaca taaccagttg attaatctgt 107460cggagcagca aatgatcgat tgtgattttg tcgacgctgg ctgtaacggc ggcttgttgc 107520acacagcgtt cgaagccatc attaaaatgg gcggcgtaca gctggaaagc gactatccat 107580acgaagcaga caataacaat tgccgtatga actccaataa gtttctagtt caagtaaaag 107640attgttatag atacattacc gtgtacgagg aaaaacttaa agatttgtta cgccttgtcg 107700gccctattcc tatggccata gacgctgccg acattgttaa ctataaacag ggtattataa 107760aatattgttt caacagcggt ctaaaccatg cggttctttt agtgggttat ggtgttgaaa 107820acaacattcc atattggacc tttaaaaaca cttggggcac ggattgggga gaggacggat 107880ttttcagggt acaacaaaac ataaacgcct gtggtatgag aaacgaactt gcgtctactg 107940cagtcattta ttaatctcaa cacactcgct atttggaaca taatcatatc gtctcagtag 108000ctcaaggtag agcgtagcgc tctggatcgt atagatcttg ctaaggttgt gagttcaagt 108060ctcgcctgag atattaaaaa actttgtaat tttaaaaatt ttattttata atatacaatt 108120aaaaactata caatttttta ttattacatt aataatgata caatttttat tattacattt 108180aatattgtct attacggttt ctaatcatac agtacaaaaa taaaatcaca attaatataa 108240ttacaaagtt aactacatga ccaaacatga acgaagtcaa tttagcggcc aattcgcctt 108300cagccatgga agtgatgtcg ctcagactgg tgccgacgcc gccaaacttg gtgttctcca 108360tggtggttat gaggttgctt ttttgttggg caataaacga ccagccgctg gcatctttcc 108420aactgtcgtg ataggtcgtg ttgccgatgg tcgggatcca aaactcgacg tcgtcgtcaa 108480ttgctagttc cttgtagttg ctaaaatcta tgcattgcga cgagtccgtg ttggccaccc 108540aacgcccttc tttgtagatg ctgttgttgt agcaattact ggtgtgtgcc ggcggattgg 108600tgcacggcat cagcaaaaac gtgtcgtccg acaaaaatgt tgaagaaaca gagttgttca 108660tgagattgcc aatcaaacgc tcgtccacct tggccacgga gactatcagg tcgtgcagca 108720tattgtttag cttgttgatg tgcgcatgca tcagctcaat gttcattttc agcaaatcgt 108780tttcgtacat cagctcctct tgaatatgca tcaggtcgcc tttggtggca gtgtctccct 108840ctgtgtactt ggctctaacg ttgtggcgcc aagtgggcgg ccgcttcttg actcggtgct 108900cgactttgcg tttaatgcat ctgttaaact tgcagttcca cgtgttttta gaaagatcat 108960atatatcatt gtcaatcaaa cagtgttcgc gtgtcaccga ctcggggtta tttttgtcat 109020ctttaatgag cagacacgca gcttttattt ggcgcgtggt gaacgtagac ttttgtttga 109080gaatcatact cacgccgtct cgatgaagca cagtgtccac ggtcacgttg atggggttgc 109140cctcagcgtc caaaatgtat acctggcact cgtccgtgtc gtcctggcac tcgagcctgc 109200tgtacatttt cgaagtggaa atgccgcatc gccacgattt gttgcacgtg tggtgcgcaa 109260agtgattgtt attctgccgc ttcaccaact ctttgccttt gacccactgg ccgcggccct 109320cgttgtcgcg aaaacagtcg tcgctgtcac tgccccaacg gtcgatcagc tcttcgccca 109380cctcgcactg ctgcctgatg ctccacataa gcaaatcctc tttgcccaca ttcagcgttt 109440tcatggtttc ttcgacgcgt gtgttgggat ccagcgagcc gccgttgtac gcatacgcct 109500ggtagtaccc cttgtagccg ataatcacgt tttcgttgta gtccgtctcc acgatggtga 109560tttccacgtc cttttgcagc gtttccttgg gcggggtaat gtccaagttt ttaatcttgt 109620acggacccgt cttcatttgc gcgttgcagt gctccgccgc aaaggcagaa tgcgccgccg 109680ccgccaaaag cacatataaa acaatagcgc ttaccatctt gcttgtgtgt tccttattga 109740agccttggtg tgactgattt actagtagca ttgaggcatc ttatataccc gaccgttatc 109800tggcctacgt gacacaaggc acgttgttag attaataatc ttatcttttt atcttaattg 109860ataagattat ttttatctgg ctgttataaa aacgggatca tgaacacgga cgctcagtcg 109920acatcgaaca cgcgcaactt catgtactct cccgacagca gtctggaggt ggtcatcatt 109980accaattcgg acggcgatca cgatggctat ctggaactaa ccgccgccgc caaagtcatg 110040tcaccttttc ttagcaacgg cagttcggcc gtgtggacca acgcggcgcc ctcgcacaaa 110100ttgattaaaa acaataaaaa ttatattcat gtgtttggtt tatttaaata tctgtcaaat 110160tacaatttaa ataataaaaa gcgtcctaaa gagtattaca cccttaaatc gattattagc 110220gacttgctta tgggcgctca aggcaaagta tttgatccgc tttgcgaagt aaaaacgcaa 110280ctgtgtgcga ttcaggagag tctcaacgag gctatttcga ttttgaacgt tcatagcaac 110340gatgcggccg ccaacccgcc tgcgccagac attaacaagt tgcaagaact gatacaagat 110400ttgcagtctg aatacaataa aaaaattacc tttaccactg atacaatttt ggagaattta 110460aaaaatataa aggatttaat gtgcctgaat aaataataat aagggttttg tacgatttca 110520acaatgaact tttgggccac gtttagcatt tgtctggtgg gttatttggt gtacgcggga 110580cacttgaata acgagctaca agaaataaaa tcaatattag tggtcatgta cgaatctatg 110640gaaaagcatt tttccaatgt ggtagacgaa attgattctc ttaaaacgga cacgtttatg 110700atgttgagca acttgcaaaa taacacgatt cgaacgtggg acgcagttgt aaaaaatggc 110760aaaaaaatat ccaatctcga cgaaaaaatt aacgtgttat taacaaaaaa cggggtagtt 110820aacaacgtgc taaacgttca ataaacgctt atcactaagt taatatacta aaaatcacat 110880agtcactaca atatttcaaa atatgaagcc gacgaataac gttatgttcg acgacgcgtc 110940ggtcctttgg atcgacacgg actacattta tcaaaattta aaaatgcctt tgcaggcgtt 111000tcaacaactt ttgttcacca ttccatctaa acatagaaaa atgatcaacg atgcgggcgg 111060atcgtgtcat aacacggtca aatacatggt ggacatttac ggagcggccg ttctggtttt 111120gcgaacgcct tgctcgttcg ccgaccagtt gttgagcaca tttattgcaa acaattattt 111180gtgctacttt taccgtcgtc gccgatcacg atcacgctca cgatcacgct cgcgatcacg 111240ttctcctcat tgcagacctc gttcgcgctc tcctcattgc agacctcgtt cgcgatctcg 111300gtcccggtct agatcgcggt cacgttcatc gtctcccagg cgagggcgtc gacaaatatt 111360cgacgcgctg gaaaagattc gtcatcaaaa cgacatgttg atgagcaacg tcaaccaaat 111420aaatctcaac caaactaatc aatttttaga attgtccaac atgatgacgg gcgtgcgcaa 111480tcaaaacgtg cagctcctcg cggcgttgga aaccgctaaa gatgttattt tgaccagatt 111540aaacacattg cttgccgaga ttacagactc gttacccgac ttgacgtcca tgttagataa 111600attagctgaa caattgttgg acgccatcaa cacggtgcag caaacctgcg caacgagttg 111660aacaacacca actctatttt gaccaattta gcgtcaagcg tcacaaacat caacggtacg 111720ctcaacaatt tgctagccgc tatcgaaaac ttagtaggcg gcggcggcgg tggcaatttt 111780aacgaagccg acagacaaaa actggacctc gtgtacactt tggttaacga aatcaaaaat 111840atactcacgg gaacgctgac aaaaaaataa gcatgtccga caaaacacca acaaaaaagg 111900gtggcagcca tgccatgacg ttgcgagagc gcggcgtaac aaaaccccca aaaaagtctg 111960aaaagttgca gcaatacaag aaagccatcg ctgccgagca aacgctgcgc accacagcag 112020atgtttcttc tttgcagaac cccggggaga gtgccgtttt tcaagagttg gaaagattag 112080agaatgcagt tgtagtatta gaaaatgaac aaaaacgatt gtatcccata ttagatacgc 112140ctcttgataa ttttattgtc gcattcgtga atccgacgta tcccatggcc tattttgtca 112200ataccgatta caaattaaaa ctagaatgtg ccagaatcag aagcgattta ctttacaaaa 112260acaaaaacga agtcgctatc aacaggccta agatatcgtc ttttaaattg caattgaaca 112320acgtaatttt agacactata gaaactattg aatacgattt acaaaataaa gttctcacaa 112380ttactgcacc tgttcaagat caagaactaa gaaaatccat tatttatttt aatattttaa 112440atagtgacag ttgggaagta ccaaagtata tgaaaaaatt gtttgatgaa atgcaattgg 112500aacctcccgt cattttacca ttaggtcttt agatttggta aggctagcac gtcgacatca 112560tgtttgcgtc gttgacctca gagcaaaagc tgttattaaa aaaatataaa tttaacaatt 112620atgtgaaaac gatcgagttg agtcaagcgc agttggctca ttggcgttca aacaaagata 112680ttcagccaaa acctttggat cgtgcagaaa ttttacgtgt cgaaaaggcc accaggggac 112740aaagcaaaaa tgagctgtgg acgctattgc gtttggatcg caacacagcg tctgcatcgt 112800ccaactcgtc cggcaacatg ttacaacgac cagcgctttt gtttggaaac gcgcaagaaa 112860gtcacgtcaa agaaaccaac ggcatcatgt tagaccacat gcgcgaaatc atagaaagta 112920aaattatgag cgcggtcgtt gaaacggttt tggattgcgg catgttcttt agccccttgg 112980gtttgcacgc cgcttcgccc gatgcgtatt tttctctcgc cgacggaacg tggatcccag 113040tggaaataaa atgtccgtac aattaccgag acacgaccgt ggagcagatg cgtgtcgagt 113100tggggaacgg caatcgcaag tatcgcgtga aacacaccgc gctgttggtt aacaagaaag 113160gcacgcccca gttcgaaatg gtcaaaacgg atgcgcatta caagcaaatg caacggcaga 113220tgtatgtgat gaacgcgcct atgggctttt acgtggtcaa attcaaacaa aatttggtgg 113280tggtttctgt gccgcgcgac gaaacgttct gcaacaaaga actgtctacg gaaaacaacg 113340cgtacgtggc gtttgccgtg gaaaactcca actgcgcgcg ctaccaatgc gccgacaagc 113400gacggctttc attcaaaacg cacagctgca atcacaacta tagtggtcaa gaaatcgatg 113460ctatggtcga tcgcggaata tatttagatt atggacattt aaaatgtgcg tactgtgatt 113520ttagctcaga cagtcgggaa acgtgcgatt ctgttttaaa acgcgagcac accaactgca 113580aaagttttaa cttgaaacat aaaaactttg acaatcctac atactttgat tatgttaaaa 113640gattgcaaag tttgctaaag agtcaccact ttagaaacga cgctaaaaca cttgcctatt 113700ttggttacta tttaactcat acaggaaccc tgaagacctt ttgctgcgga tcgcaaaact 113760cgtcgcccac caaacacgat catttaaacg actgtgtata ttatttggaa ataaaataaa 113820cctttatatt atatataatt cttttattta tacatttgtt tatacaattt tatttacgac 113880aaatattgac tcgttgttca gaaagtttaa taagcttgtc aatttcttcg gcttgcaaag 113940ggctgccaac gcgttcgttt tgaatgcgcg taatccggtt tacggtattg ttggcgcgaa 114000caataaactc ctcaactggc aaattaacaa ttttgtttgc gtactcattg tgcactgcgg 114060ccaggttttg tagaatgttt tcgggaaaaa tggcaattct attaaatttg acatgttttt 114120gattgtatac atagttttga tattcttcca gcgtaggata tttgtttaaa ctcttgacgc 114180attcaatgta caatttgtgc agtgacaaaa ttctgttaaa atccaaacga gaacatttct 114240caaaagttat ttcttgaccg ttgaaatgta cactttgcaa ttgtttcaat aaactgtcgt 114300aaaaagtttt tccttcttca agcacaaacg cggggcgcat cgtgttatct acaacgctta 114360tgtacttgtc aaaatcttca attatatgat agaaatacaa atatctctcc gcgtttatgg 114420acgtgtcgtt taaaacatgt tcgtcaacaa ctccgttatg atttactttc aaaaatttca 114480aatcttgcaa agcgtccgcg ttggtcaact tgttgataat aaatttgtct ttgcattcaa 114540acgctctgtt tgcaatccac tccacagcgt ccaaaacgga catgcgttta aacatgttga 114600tacgttttag acaatacgct cgttttttta ccgcctcaac gttcacgtcc gtgtagtcgc 114660accattgcag gatttgcaac atgtcctcgg caaaatgcgc gaactgccgc agcttttcct 114720ttccaaaatg ttgattgtcg tgtttaaaaa gcaacgttga aatttccgag acataccaca 114780aagccgtggg caattttact ttgatcagcg gctccatagc caggttgctg aacccgatca 114840tgcattccgt gttgttaatg cggtaaatga catagcgttt aaagtagtcc tttacattat 114900cgtcaatgta ttctgcgtcg tttatgtgct tgtacagcaa atagtacata aggcccgcgt 114960taaacgcgac ctttttagcg tcaaaatacg tgcacgccaa cacgtaatcg ttgtattcgt 115020cgaattgctc gttgggcact atggcgcccg taaaagggcg tctgctgcgc ggtgacaaac 115080gcgttccatg ctgaatcaac tgcttcaaac tttccaaatt ataacaatat tcaattgaat 115140ttttaatctc tttattttgg ctccataaaa gaggaaactc gagtcggctt ttaaacttgg 115200tcaaactgcc ctgaattgtt tcaaacaagt tgtaatgtgt taacaatatg gccggcacac 115260cgctatcgtt ggctaaaata caatcgggga atcgaatatt ttctacgttg ctgtaatcgt 115320acgcttcgtc gtcgtcgttg gcaacaacat cgtcggtttc ggcgttaacg ctcgctaact 115380tgttctgata gtgtaaattt ttcattacat caaaagcgta tgacttgttg cgattgtgca 115440aataatttat ggccgtgcta atggtgctgt cgataatttt atcaaaattg agaacatcgg 115500cgttatacaa cgttttataa aattctgttg acttgaacgt gtttacaaac tcatttttat 115560ttttaatctg gtcaaaattc atactagaat tgttagtttg tttgatttcg ctgaatagcc 115620gctggcggag acgcttcagc ttgtccacct cgtttaacac gttggcgtcc gtcggcatgg 115680aattgataaa tttgaaccga acaaaagaca gcagttcatc ttttttcgat ataaaatttt 115740cggttgtaat gatatcgtag ttaaattctt tggttaaatt gacccattcg accatttcat 115800cgttgcgata aatcttgcag tccgagttgt tgacaaacgc cgaggcaacg gacaaatcaa 115860tctgttccgt gttattattg atggcataaa acacaatgcg ttcgaaacta aacggttttt 115920cgtttagcaa atttttgcaa acgtttgcct catttttgga aatttggccg tcggtcacca 115980tgtacaaaag tttcaacttg ccgtcgagca agtttatatt cttgtgaatc cactttatga 116040attcgctggg cctggtgtca gtaccctcgc cattgcggcg caaataacga ctcttgacgt 116100ctccgatttc tttttggcgg caataagcac tccaatgcaa atacaaaact ttgtcgcaac 116160tactgatgtt ttcgatttca ttctgaaatt gttctaaagt ttgtaacgcg ttcttgttaa 116220agtaatagtc cgagtttgtc gacaaggaat cgtcggtggc gtacacgtag tagttaatca 116280tcttgttgat tgatatttaa ttttggcgac ggatttttat atacacgagc ggagcggtca 116340cgttctgtaa catgagtgat cgtgtgtgtg ttatctctgg cagcgcgata gtggtcgcga 116400aaattacacg cgcgtcgtaa cgtgaacgtt tatattataa atattcaacg ttgcttgtat 116460taagtgagca tttgagcttt accattgcaa aatgtgtgta atttttccgg tagaaatcga 116520cgtgtcccag acgattattc gagattgtca ggtggacaaa caaaccagag agttggtgta 116580cattaacaag attatgaaca cgcaattgac aaaacccgtt ctcatgatgt ttaacatttc 116640gggtcctata cgaagcgtta cgcgcaagaa caacaatttg cgcgacagaa taaaatcaaa 116700agtcgatgaa caatttgatc aactagaacg cgattacagc gatcaaatgg atggattcca 116760cgatagcatc aagtatttta aagatgaaca ctattcggta agttgccaaa atggcagcgt 116820gttgaaaagc aagtttgcta aaattttaaa gagtcatgat tataccgata aaaagtctat 116880tgaagcttac gagaaatact gtttgcccaa attggtcgac gaacgcaacg actactacgt 116940ggcggtatgc gtgttgaagc cgggatttga gaacggcagc aaccaagtgc tatctttcga 117000gtacaacccg attggtaaca aagttattgt gccgtttgct cacgaaatta acgacacggg 117060actttacgag tacgacgtcg tagcttacgt ggacagtgtg cagtttgatg gcgaacaatt 117120tgaagagttt gtgcagagtt taatattgcc gtcgtcgttc aaaaattcgg aaaaggtttt 117180atattacaac gaagcgtcga aaaacaaaag catgatctac aaggctttag agtttactac 117240agaatcgagc tggggcaaat ccgaaaagta taattggaaa attttttgta acggttttat 117300ttatgataaa aaatcaaaag tgttgtatgt taaattgcac aatgtaacta gtgcactcaa 117360caaaaatgta atattaaaca caattaaata aatgttaaaa tttattgcct aatattattt 117420tgtcattgct tgtcatttat taatttggat gatgtcattt gtttttaaaa ttgaactggc 117480tttacgagta gaattctacg cgtaaaacac aatcaagtat gagtcataat ctgatgtcat 117540gttttgtaca cggctcataa ccgaactggc tttacgagta gaattctact tgtaatgcac 117600gatcagtgga tgatgtcatt tgtttttcaa atcgagatga tgtcatgttt tgcacacggc 117660tcataaactc gctttacgag tagaattcta cgtgtaacgc acgatcgatt gatgagtcat 117720ttgttttgca atatgatatc atacaatatg actcatttgt ttttcaaaac cgaacttgat 117780ttacgggtag aattctactt gtaaagcaca atcaaaaaga tgatgtcatt tgtttttcaa 117840aactgaactc gctttacgag tagaattcta cgtgtaaaac acaatcaaga aatgatgtca 117900tttgttataa aaataaaagc tgatgtcatg ttttgcacat ggctcataac taaactcgct 117960ttacgggtag aattctacgc gtaaaacatg attgataatt aaataattca tttgcaagct 118020atacgttaaa tcaaacggac gttatggaat tgtataatat taaatatgca attgatccaa 118080caaataaaat tgtaatagag caagtcgaca atgtggacgc gtttgtgcat attttagaac 118140cgggtcaaga agtgttcgac gaaacgctaa gccagtacca ccaatttcct ggcgtcgtta 118200gttcgattat tttcccgcaa ctcgtgttaa acacaataat tagcgttttg agcgaagacg 118260gcagtttgct cacgttgaaa ctcgaaaaca cttgttttaa ttttcacgtg tgcaataaac 118320gctttgtgtt tggcaatttg ccagcggcgg tcgtgaataa tgaaacgaag caaaaactgc 118380gcattggagc tccaattttt gccggcaaaa agctggtttc ggtcgtgacg gcgtttcatc 118440gtgttggcga aaacgaatgg ctgttaccgg tgacgggaat tcgagaggcg tcccagctgt 118500cgggacatat gaaggtgctg aacggcgtcc gtgttgaaaa atggcgaccc aacatgtccg 118560tctacgggac tgtgcaattg ccgtacgata aaattaaaca gcatgcgctc gagcaagaaa 118620ataaaacgcc aaacgcgttg gagtcttgtg tgctatttta caaagattca gaaatacgca 118680tcacttacaa caagggggac tatgaaatta tgcatttgag gatgccggga cctttaattc 118740aacccaacac aatatattat agttaaataa gaattattat caaatcattt gtatattaat 118800taaaatacta tactgtaaat tacattttat ttacaatcat gtcaaagcct aacgttttga 118860cgcaaatttt agacgccgtt acggaaacta acacaaaggt tgacagtgtt caaactcagt 118920taaacgggct ggaagaatca ttccagcttt tggacggttt gcccgctcaa ttgaccgatc 118980ttaacactaa gatctcagaa attcaatcca tattgaccgg cgacattgtt ccggatcttc 119040cagactcact aaagcctaag ctgaaaaccc aagcttttga actcgattca gacgctcgtc 119100gtggtaaacg cagttccaag taaatgaatc gtttttaaaa taacaaatca attgttttat 119160aatattcgta cgattctttg attatgtaat aaaatgtgat cattaggaag attacgaaaa 119220atataaaaaa tatgagttct gtgtgtataa caaatgctgt aaacgccaca attgtgtttg 119280ttgcaaataa acccagtatt atttgattaa aattgttgtt ttctttgttc atagacaata 119340gtgtgttttg cctaaacgtg tactgcataa actccatgcg agtgtatagc gagctagtgg 119400ctaacgcttg ccccaccaaa gtagattcgt caaaatcctc aatttcatca ccctcctcca 119460agtttaacat ttggccgtcg gaattaactt ctaaagatgc cacataatct aataaatgaa 119520atagagattc aaacgtggcg tcatcgtccg tttcgaccat ttccgaaaag aactcgggca 119580taaactctat gatttctctg gacgtggtgt tgtcgaaact ctcaaagtac gcagtcagga 119640acgtgcgcga catgtcgtcg ggaaactcgc gcggaaacat gttgttgtaa ccgaacgggt 119700cccatagcgc caaaaccaaa tctgccagcg tcaatagaat gagcacgatg ccgacaatgg 119760agctggcttg gatagcgatt cgagttaacg ctttggcagt cacggtcagc gttttgatgg 119820cgatcacgtt gagcgagtgc actaacgcgg ctttgtaagt ctctcccaac atgcgcacgg 119880tcacgcgccg agtcgtgcta agcaacatgt gtttcatggc cggaatgaga gaagtgttaa 119940tttttttcaa catgctttta aacccggaca ttagcatatc aaagccaatg tccgtagcaa 120000taccgaaaac gagcgcgtaa tcttccaaaa acgatgttat aattgactcc aagtcttggt 120060cgctgattga acggtcgagc gcctcgaaat gttcgacacg tgcacgttcg ttaccgcggt 120120aattgtatgc gatcggagtt ttagtaaagc cggtttcggc cgtgtacgtg atctggacgg 120180gcgacccgtt gacgatcatg cccaaatcgt ttagtgttgg atttttgtta aaaagttttt 120240caaattccaa gtctgtggcg ttatcgcgca cgctgcgcca ttgcgctagt attgcgttgg 120300agtccacgtt gggtcgtggc ggtagtatgc tggaaggcgc tttgtaatca aaatcgcgca 120360gttcgctaaa aatgttgttg gccagcattt tgaaagtgac aaagatcgtg tcgcccagca 120420cgaatccgat

gagcgattcc caccatctaa acgaacaacc gccgttgaat agctctctgc 120480cgaaacgtcg acagtaggct tcgttgaatt cgcctttaaa gcgttcggga aacaaggggt 120540cgggatcggg ccgaacgtta aaagccggca catcgtccac gcccatgatc gtgtgttctt 120600cggtgcgcaa gtatgggctg ttaaagtaca ttttggacag cgagtccact aagatgcatt 120660tgttgtcgag cgtgtatcta aactcggcag actgaacttg ggtttcggcg ccttcacgca 120720tggccgccgc cctgtccagg tggtagcacg cgggctgcgc gtaacccacg ctagtctcgg 120780aggtctgcat gtacatgaac ggcgtcgtgt tggacacgac gccggtttcg tgaaacggat 120840agcagctcat gcttacacac ccgcgcttgc tgaaagccag tttgacggcc agcgctttgt 120900cggccaattt cggcggcaca taataatcgt cgtcacttga cgcgggacgc agcgtgtagt 120960cgattagtat atgcggaaac ctggtgcgcc atctcgaaat aaactcgaga cgatgcatat 121020gtatggcata cctactggca ttagttaaat cgacggctgt taaaaccgcc atgttatata 121080ggacttaaaa taaacaacaa tatataatga aatatttatt agattatatt atagcaatac 121140atttacattt attataacaa tactttttat ttaatctgat tatattataa cgatacattt 121200ttatttagac attgttattt acaatattaa ttaacttttt atacattttt aaatcataat 121260atataatcat ttcgttgtgc atttcaaagc ttttgatagc ttcaaagtaa tacatgaatt 121320tagagtattc aggaaaatga taaacgttgg taaacccgca tttggtacaa tataacacgg 121380gatttttata atacagttta gtttttttac acaatttgca atagttgtta gttgtaggtt 121440tcaaaggaaa cgtgattgcg ccgtccaata cctgggtaaa ctttttgact ttaacagtgg 121500caaacacggt tcctttgata cccgaaaatc ggttgtcttg cagagcggcc atcatttcgc 121560ttggctcttg aagtataaaa cagttgacgt catccaccac gtcgggtctg gtgcacatgc 121620ttcggtagcg ctgcaacact atattggtgt atgtttccct gagaacgaga ccgccggtgg 121680tgctaagatc gattgtttga atgcgctcgt tgggctcttt gtgatttcga attatgcgcc 121740gaattatttc aaacactttg cagttgtgat cgtcaattct caattcttta acttccgtcg 121800tgtgctctaa acttacaggg aaaatgtatt ggtaaaaaaa cctctctctg gctaaatagc 121860tgaggtcgac caaattgata gaaggatata tttcgtacga ggtttttgga acgttgtgat 121920atagatagca tttttgacag cagatgtcta tgcggtcagg atcgtccaac ggcttttcga 121980tgtgaaccac aacatacaaa aaccattcgc gcgtgttgtc tttgaatcta taattgcaag 122040tggtgcatcg cgaatcgctc atgtgctcca tagtcttctt gtatttcaca ggcctgcttg 122100caaatttgcc cgtcatgcgc atatctttgc tgtttatgta gcccataatg taattggtgg 122160aaaattttag cgtggctttc atgatgtcgc gttctaaatc gctcatgaaa tgcatacgta 122220gatcgcgctc ttgtttgaaa tccagtttgt cgctgtacgc gggcaaacct tcaaacttgt 122280tcccaaactc gggcggcaca aaatatccat cttttctgtt gacgactggt tttttactta 122340caatgctgct gtgctccaac ggcttggccg gagaggtgca cataggctgt ttaggcggag 122400agatgcgcgt aggtggtttg atgttagatt ttggcggcgg acgaacaggc gacggcggcg 122460agttggcggc aggcgctggc aaagatttgg cacgaccctt gcccccggtc cttggcgcgt 122520caaaaatgtt attctctcga aaaaaacggt tcattgtaac tgttagttag cactcagaaa 122580tcaacacgat actgtgcacg ttcagccatc gagaggcttt atatatggaa accttatcta 122640tagagataag attgtatatg cgtaggagag cctggtcacg taggcacttt gcgcacggca 122700ctagggctgt ggaggggaca ggctatataa agcccgtttg cccaactcgt aaatcagtat 122760caattgtgct ccggcgcaca cgctcgcttg cgcgccggat agtataagta attgataacg 122820ggcaacgcaa catgataaga accagcagtc acgtgctgaa cgtccaggaa aatataatga 122880cgtcaaactg tgcgtcatcg ccatattcgt gcgaggcaac gtccgcttgc gcagaagctc 122940agcaggtaat gatcgataac tttgttttct ttcacatgta caacgccgac atacaaattg 123000acgcaaagct gcaatgcggc gtgcgctcgg ccgcgtttgc aatgatcgac gataaacatt 123060tggaaatgta caagcataga atagagaata aattttttta ttactatgat caatgtgccg 123120acattgccaa acccgaccgt ctgcccgatg acgacggcgc gtgctgtcac cattttattt 123180ttgatgccca acgtattatt caatgtatta aagagattga aagcgcgtac ggcgtgcgtg 123240atcgcggcaa tgtaatagtg ttttatccgt acttgaaaca gttgcgagac gcgttgaagc 123300taattaaaaa ctcttttgcg tgttgtttta aaattataaa ttctatgcaa atgtacgtga 123360acgagttaat atcaaattgc ctgttgttta ttgaaaagct ggaaactatt aataaaactg 123420ttaaagttat gaatttgttt gtagacaatt tggttttgta cgaatgcaat gtttgtaaag 123480aaatatctac ggatgaaaga tttttaaagc caaaagaatg ttgcgaatac gctatatgca 123540acgcgtgctg cgttaacatg tggaagacgg ccaccacgca cgcaaaatgt ccagcgtgca 123600ggacatcgta taaataagca cgcaacgcaa aatgagtggt ggcggcaact tgttgactct 123660ggaaagagat cattttaaat atttattttt gaccagctat tttgatttaa aagataatga 123720acatgttcct tcagagccta tggcatttat tcgcaattac ttgaattgca cgtttgattt 123780gctagacgat gccgtgctca tgaactattt caattacttg caaagcatgc aattgaaaca 123840tttggtgggc agcacgtcga caaacatttt caagtttgta aagccacaat ttagatttgt 123900gtgcgatcgc acaactgtgg acattttaga atttgacacg cgcatgtaca taaaacccgg 123960cacgcccgtg tacgccacga acctgttcac gtccaatccc cgcaagatga tggctttcct 124020gtacgctgaa tttggcaagg tgtttaaaaa taaaatattc gtaaacatca acaactacgg 124080ctgcgtgttg gcgggcagtg ccggtttctt gttcgacgat gcgtacgtgg attggaatgg 124140tgtgcgaatg tgtgcggcgc cgcgattaga taacaacatg catccgttcc gactgtatct 124200actgggcgag gacatggcta agcactttgt cgataataat atactaccgc cgcacccttc 124260taacgcaaag actcgcaaaa tcaacaattc aatgtttatg ctgaaaaact tttacaaagg 124320tctgccgctg ttcaaatcaa agtacacggt ggtgaacagc actaaaatcg tgacccgaaa 124380acccaacgat atatttaatg agatagataa agaattaaat ggcaactgtc cgtttatcaa 124440gtttattcag cgcgactaca tattcgacgc ccagtttccg ccagatttgc ttgatttgct 124500aaacgaatac atgaccaaaa gctcgatcat gaaaataatt accaagtttg tgattgaaga 124560aaaccccgct atgagcggtg aaatgtctcg cgagattatt cttgatcgct actcagtaga 124620caattatcgc aagctgtaca taaaaatgga aataaccaac cagtttcctg tcatgtacga 124680tcatgaatcg tcgtacattt ttgtgagcaa agactttttg caattgaaag gcactatgaa 124740cgcgttctac gcgcccaagc agcgtatatt aagtattttg gcggtgaatc gtttgtttgg 124800cgccacggaa acgatcgact ttcatcccaa cctgctcgtg taccggcaga gttcgccgcc 124860ggtccgtttg acgggcgacg tgtatgttgt tgataagaac gaaaaagttt ttttggtcaa 124920acacgtgttc tcaaacacgg tgcctgcata tcttttaata agaggtgatt acgaaagttc 124980gtctgacttg aaatcccttc gcgatttgaa tccgtgggtt cagaacacgc ttctcaaatt 125040attaatcccc gactcggtac aataatatga tttacactga tcccactact ggcgctacga 125100ctagcacaga cgtcgtccgt ccacaaacta tttaaacagg ctaactccaa acatgttctt 125160gaccatcttg gctgtagtag taattattgc tttaataatt atatttgttc aatctagcag 125220taatggaaac agctcggggg gtaatgtacc tccaaacgcc ctggggggtt ttgtaaatcc 125280tttaaacgct accatgcgag ctaatccctt tatgaacacg cctcaaaggc aaatgttgta 125340gataagtgta taaaaaatga aacgtatcaa atgcaacaaa gttcgaacgg tcaccgagat 125400tgtaaacagc gatgaaaaaa tccaaaagac ctacgaattg gctgaatttg atttaaaaaa 125460tctaagcagt ttagaaagct atgaaactct aaaaattaaa ttggcgctca gcaaatacat 125520ggctatgctc agcaccctgg aaatgactca accgctgttg gaaatattta gaaacaaagc 125580agacactcgg cagattgccg ccgtggtgtt tagcacatta gcttttatac acaatagatt 125640ccatcccctt gttactaatt ttactaacaa aatggagttt gtggtcactg aaaccaacga 125700cacaagcatt cccggagaac ccattttgtt tacggaaaac gaaggtgtgc tgctgtgttc 125760cgtggacaga ccgtctatcg ttaaaatgct aagccgcgag tttgacaccg aggctttagt 125820aaactttgaa aacgacaact gcaacgtgcg gatagccaag acgtttggcg cctctaagcg 125880caaaaacacg acgcgcagcg atgattacga gtcaaataaa caacccaatt acgatatgga 125940tttgagcgat tttagcataa ctgaggttga agccactcaa tatttaactc tgttgctgac 126000cgtcgaacat gcctatttac attattatat ttttaaaaat tacggggtgt ttgaatattg 126060caaatcgcta acggaccatt cgctttttac caacaaattg cgatcgacaa tgagcacaaa 126120aacgtctaat ttactgttaa gcaaattcaa atttaccatt gaagattttg acaaaataaa 126180ctcaaattct gtaacatcag ggtttaatat atataatttt aataaataat taaataatat 126240acaatgtttt tattaattat atttttaata ttaattaaaa gtattaatat ttaaaaaaat 126300gaatcaaatt catctaaagt gtcacagcga taaaatttgt cctaaagggt attttggcct 126360caacgccgat ccctatgatt gcacggcgta ttatctgtgt ccgcataaag tgcaaatgtt 126420ttgcgaatta aatcacgaat ttgacttgga ctccgccagc tgcaagccta tcgtgtacga 126480tcacacgggc agcgggtgta cggctcgcat gtatagaaac ttgttactat gaagagcggg 126540tttccagttg cacaacacta ttatcgattt gcagttcggg acataaatgt ttaaatatat 126600cgatgtcttt gtgatgcgcg cgacattttt gtaggttatt gataaaatga acggatacgt 126660tgcccgacat tatcattaaa tccttggcgt agaatttgtc gggtccattg tccgtgtgcg 126720ctagcatgcc cgtaacggac ctcgtacttt tggcttcaaa ggttttgcgc acagacaaaa 126780tgtgccacac ttgcagctct gcatgtgtgc gcgttaccac aaatcccaac ggcgcagtgt 126840acttgttgta tgcaaataaa tctcgataaa ggcgcggcgc gcgaatgcag ctgatcacgt 126900acgctcctcg tgttccgttc aaggacggtg ttatcgacct cagattaatg tttatcggcc 126960gactgttttc gtatccgctc accaaacgcg tttttgcatt aacattgtat gtcggcggat 127020gttctatatc taatttgaat aaataaacga taaccgcgtt ggttttagag ggcataataa 127080aagaaatatt gttatcgtgt tcgccattag ggcagtataa attgacgttc atgttggata 127140ttgtttcagt tgcaagttga cactggcggc gacaagatcg tgaacaacca agtgactatg 127200acgcaaatta attttaacgc gtcgtacacc agcgcttcga cgccgtcccg agcgtcgttc 127260gacaacagct attcagagtt ttgtgataaa caacccaacg actatttaag ttattataac 127320catcccaccc cggatggagc cgacacggtg atatctgaca gcgagactgc ggcagcttca 127380aactttttgg caagcgtcaa ctcgttaact gataatgatt tagtggaatg tttgctcaag 127440accactgata atctcgaaga agcagttagt tctgcttatt attcggaatc ccttgagcag 127500cctgttgtgg agcaaccatc gcccagttct gcttatcatg cggaatcttt tgagcattct 127560gctggtgtga accaaccatc ggcaactgga actaaacgga agctggacga atacttggac 127620aattcacaag gtgtggtggg ccagtttaac aaaattaaat tgaggcctaa atacaagaaa 127680agcacaattc aaagctgtgc aacccttgaa cagacaatta atcacaacac gaacatttgc 127740acggtcgctt caactcaaga aattacgcat tattttacta atgattttgc gccgtattta 127800atgcgtttcg acgacaacga ctacaattcc aacaggttct ccgaccatat gtccgaaact 127860ggttattaca tgtttgtggt taaaaaaagt gaagtgaagc cgtttgaaat tatatttgcc 127920aagtacgtga gcaatgtggt ttacgaatat acaaacaatt attacatggt agataatcgc 127980gtgtttgtgg taacttttga taaaattagg tttatgattt cgtacaattt ggttaaagaa 128040accggcatag aaattcctca ttctcaagat gtgtgcaacg acgagacggc tgcacaaaat 128100tgtaaaaaat gccatttcgt cgatgtgcac cacacgttta aagctgctct gacttcatat 128160tttaatttag atatgtatta cgcgcaaacc acatttgtga ctttgttaca atcgttgggc 128220gaaagaaaat gtgggtttct tttgagcaag ttgtacgaaa tgtatcaaga taaaaattta 128280tttactttgc ctattatgct tagtcgtaaa gagagtaatg aaattgagac tgcatctaat 128340aatttctttg tatcgccgta tgtgagtcaa atattaaagt attcggaaag tgtgcagttt 128400cccgacaatc ccccaaacaa atatgtggtg gacaatttaa atttaattgt taacaaaaaa 128460agtacgctca cgtacaaata cagcagcgtc gctaatcttt tgtttaataa ttataaatat 128520catgacaata ttgcgagtaa taataacgca gaaaatttaa aaaaggttaa gaaggaggac 128580ggcagcatgc acattgtcga acagtatttg actcagaatg tagataatgt aaagggtcac 128640aattttatag tattgtcttt caaaaacgag gagcgattga ctatagctaa gaaaaacaaa 128700gagttttatt ggatttctgg cgaaattaaa gatgtagacg ttagtcaagt aattcaaaaa 128760tataatagat ttaagcatca catgtttgta atcggtaaag tgaaccgaag agagagcact 128820acattgcaca ataatttgtt aaaattgtta gctttaatat tacagggtct ggttccgttg 128880tccgacgcta taacgtttgc ggaacaaaaa ctaaattgta aatataaaaa attcgaattt 128940aattaattat acatatattt tgaatttaat taattataca tatattttat attatttttg 129000tcttttatta tcgaggggcc gttgttggtg tggggttttg catagaaata acaatgggag 129060ttggcgacgt tgctgcgcca acaccacctc ctcctcctcc tttcatcatg tatctgtaga 129120taaaataaaa tattaaacct aaaaacaaga ccgcgcctat caacaaaatg ataggcatta 129180acttgccgct gacgctgtca ctaacgttgg acgatttgcc gactaaacct tcatcgccca 129240gtaaccaatc tagacccaag tcgccaacta aatcaccaaa cgagtaaggt tcgatgcaca 129300tgagtgtttg gcccgcagga agatcgctaa tatctacgta ttgaggcgaa tctgggtcgg 129360cggacggatc gctgccgcga caaactgttt tttctacttc atagttgaat ccttggcaca 129420tgttggttag ttcgggcgga ttgttaggca acaaggggtc gaatgggcaa atggtaacat 129480ccgactgatt tagattgggg tcttgacgac aagtgcgctg caataacaag caggcctcgg 129540cgatttctcc ggcgtcttta ccttgcacat aataacttcc gccggtgtta ttgatggcgt 129600tgattatatc ttgtactagt gtggcggcgc taaacaagaa atagccgccg gtggccaaga 129660gtatgcccgt tcctcctact tttaagcttt gcatgtaact atgtagacgg gggttttgct 129720gcagtgcgtt ttgaacacct tcgggcgtgc gcacgttggt ttccgggaag ttttgtttga 129780ctgcattgga tcgcgtctgc ttggtgtggt aattaaagtc tggcacgttg tccacgcgcc 129840gcaattggct caatgagttt atttgagggt ctgaaatgcc ctgaaatact ccgcgtatgt 129900tggggacatc attgttacga gtaattctgt ttatgtctga agtgctcaca aactggttgt 129960tagatagttg atagcccggc tgaaatctgt tgtttccaat gttgcgtaca ctgggcgcgt 130020tgagcacatt tgtgaaaccg gcgggagtgc ttgttaaaag acgcgtatta tcagtaataa 130080aactggcctg attaggatac aatttattga ctgcgcgaag atttgaaaaa aaactcattt 130140taaagcaaac ttatttaata aatatatcac agtaaaggtt ttgcaaaact gccgtcgtca 130200atacaacacg gcagcggcgt catgttggta aaatctaatc ttctccttgc tttagattct 130260gggcgagaag gcgcatttgt tgtgtaagtt atttcgacgt ctgcattatt tgttgtgtaa 130320ggtatctcga cgtatgaagc aactttaaca ttgttataat tttttttaaa tattgatgcg 130380ctccacggcg cgcgttgata cggatgatat ctctccattg tatgatcgct aaatttatat 130440accgtttcaa taaatatgtt aaaacccaac atgttaatta taatattcat aatagtttgt 130500ttgttttcaa taattatttt tactgttttg aaatctaaaa gaggtgacga tgacgaatca 130560gacgacgggt tcagttgcta taacaaacca attggagtaa attttccgca tcctactaga 130620tgtgacgctt tctacatgtg tgtcggttta aatcaaaaat tagagttaat ctgccctgaa 130680ggatttgaat ttgatccaga tgttaaaaat tgtgttccta tatcagatta tggatgtacc 130740gctaaccaaa actaaaaata aaataaaatt tatatagatt aatgaaataa aatttatata 130800gattaataaa ataaaattta tttaatatat tatactattt atattattta caacacttaa 130860cgtctagaca taacagtttg taacttagaa actaaatcag agttactgcg ctcaaactct 130920gaaaatttgg cttgagactc ggccacctgc ttacgcaatt gttcttgcag attattcaca 130980gtcgattgca actcttctga tttcttggta gattcttgca agtcatagtt tgccttttgt 131040aaatctaatt cggcgacagc atgcttgtgt ttaagcataa tgtagtcgct gtttaacatg 131100gtcattttat gttcaacttg gctggtcttg gctcgcagct cggacagttc tttttgcaat 131160tgctccacat agttcaagtc cgtggtgtga ttgttgaccg tgttattttc taaaagctcg 131220cgccaatgct gtttgatgga atcctggtta cgagtgacgt taatgggcat aaattctaca 131280tacccgtgct tattgtacac gcgacaatct gatgaagtag cgctgcaaaa acatttgtac 131340acagaattgt ccataattat cttgacataa cacttgaaac acacagcatg gttacaatga 131400atcgaagtca caaacgagga atttacgttt ttagtgtctt taaaagtagt aaaacaaata 131460ttacacgaaa cctctacttc ttcttcgggt tctgattgct gctgctgctg ctgctgcggc 131520tgcggagact gcggcgaggc aaacaaatct ggcgactgtg gtattacgta attcggcgaa 131580taagatggac tataagtggg agaccttggg gcaatctcat tcatcagctg agcctcaaga 131640tctaaacctc gttgcagagc cctctgcgca gctgtctccg acgcaatgtt atcctggtac 131700tgctgggcag tgatgtcggg aaaccgttca cgatccacat tttcactatt aattagtatg 131760acgtcatcct cttgacttaa tagcggatcg tcattgctaa tgttaacctg accgtgcacg 131820taatacgtga caccctgacg atggtaggtg cgcgtcaacg gctcgttgac gttcccgata 131880atctgcacgt tttcttcgct gacacgctgc tcctgacgcc gctcctgacg gcgatggctg 131940cgactgcttg aagacggctg gctgcgactg cttgaagacg gctgggcttc gggagatgtt 132000gtaaagttga tgcggcgacg gctgagagac agcctgtggc ggcggctgct gctgggagtg 132060gcggcgttga tttggcgact catggctggg ctggtaggat actgttcact aggctgtgag 132120gcttgaactg tgcttacgag tagaacggca gctgtattta tactgtttat cagtactgca 132180cgactgataa gacaatagtg gtgggggaac ttgccaggca aaaatgaact tttttgtaat 132240gcaaaaaagt tgatagtgta gtagtatatt gggagcgtat cgtacagtgt agactattct 132300aataaaatag tctacgattt gtagagattg tactgtatat ggagtgtcag gcaaaagtga 132360acttttttgc attgcaaaaa aattcatttt aaatttatca tatcacaggc tgcagtttct 132420gttatctgtc ccccactcag gcgtgcagct ataaaagcag gcactcacca actcgtaagc 132480acagttcgtt gtgaagtgaa cacggagagc ctgccaataa gcaaaatgcc aagggacacc 132540aacaatcgcc accggtctac gccatatgaa cgtcctacgc ttgaagatct ccgcagacag 132600ttgcaagaca atttggacag cataaaccgc cgagacagaa tgcaagaaga acaagaagaa 132660aacctgcgct atcaagtgcg tagaaggcag cgtcaaaacc agctccgctc catacaaatg 132720gaacagcagc gaatgatggc ggaattaaac aacgagccgg tgattaattt taaatttgag 132780tgtagtgtgt gtttagaaac atattcccaa caatctaacg atacttgtcc ttttttgatt 132840ccgactacgt gcgaccacgg tttttgtttc aaatgcgtca tcaatctgca aagcaacgcg 132900atgaatattc cgcattccac tgtgtgctgt ccattgtgca atacccaggt aaaaatgtgg 132960cgttccttaa agcctaacgc tgttgtgacg tgtaagtttt acaagaaaac tcaagaaaga 133020gttccgcccg tgcagcagta taaaaacatt attaaagtgc tacaagaacg gagcgtgatt 133080agtgtcgaag acaacgacaa taattgtgac ataaatatgg agaatcaggc aaagatagct 133140gctttggaag ctgaattgga agaagaaaaa aatcacagtg atcaagtagc ttctgaaaac 133200cgacagctga tagaagaaaa tactcgtctc aatgaacaga ttcaagagtt gcagcatcag 133260gtgaggacat tggtgccgca acgtggcatt acggttaatc agcaaattgg ccgtgacgac 133320agtgcgccag ccgagctgaa cgagcgtttt cgctcacttg tctattcgac tatttcagag 133380ctgtttattg aaaatggcgt tcatagtatt caaaattatg tttatgccgg aacttctgct 133440gctagttcat gtgatgtaaa tgttactgtt aattttgggt ttgaaaatta atgtgatatg 133500aaatgtatat ataaaaatga tggaataaat aataaacatt tttatacttt ttatgttttt 133560tttatttcat gtgattaaga aacttttaag atggatagta gtaattgtat taaaatagat 133620gtaaaatacg atatgccgtt acattatcaa tgtgacaata acgcagataa agacgttgta 133680aatgcgtatg acactatcga tgttgacccc aacaaaagat ttataattaa tcataatcac 133740gaacaacaac aagtcaatga aacaaataaa caagttgtcg ataaaacatt cataaatgac 133800acagcaacat acaattcttg cataataaaa atttaaatga catcatattt gagaataaca 133860aatgacatta tccctcgatt gtgttttaca agta 133894245DNAartificialvp39-F forward primer 2gcttctaata cgactcacta tagggtcgta tccgctaagc gttct 45345DNAartificialvp39-R reverse primer 3gcttctaata cgactcacta tagggacgca acgcgttata cacag 45443DNAartificial45510 forward primer 4cttctaatac gactcactat agggacagcg tgtacgagtg cat 43545DNAartificial46235 reverse primer 5gcttctaata cgactcacta tagggatctc gagcgtgtag ctggt 45644DNAartificial90292 forward primer 6gcttctaata cgactcacta tagggtaccg ccgaacatta cacc 44743DNAartificial90889 reverse primer 7gcttctaata cgactcacta tagggtctat tggcacgttt gct 43845DNAartificialec-27-F forward primer 8gcttctaata cgactcacta tagggaaagc agacactcgg cagat 45945DNAartificialec-27-R reverse primer 9gcttctaata cgactcacta tagggttgag tggcttcaac ctcag 451044DNAartificialdbp-F forward primer 10gcttctaata cgactcacta tagggcgctc gctagttttg ttct 441144DNAartificialdbp-R reverse primer 11gcttctaata cgactcacta tagggaaaga tcggaaggtg gtga 441245DNAartificialgfp-F forward primer 12gcttctaata cgactcacta tagggctgac cctgaagttc atctg 451344DNAartificialgfp-R reverse primer 13gcttctaata cgactcacta tagggaactc cagcaggacc atgt 441445DNAartificialcat-F forward primer 14gcttctaata cgactcacta tagggacggc atgatgaacc tgaat 451545DNAartificialcat-R reverse primer 15gcttctaata cgactcacta tagggatccc aatggcatcg taaag 451668DNAartificialvp80-KO-F forward primer 16ctgtattgta atctgtaagc gcacatggtg cattcgatat aaccttataa tgtgtgctgg 60aatgccct

681771DNAartificialvp80-KO-R reverse primer 17aaatgtactg aatataaata aaaattaaaa atattttata attttttatt taccgttcgt 60atagcataca t 711821DNAartificial89507 forward primer 18agcggtcgta aatgttaaac c 211925DNAartificial91713 reverse primer 19tgtataaaca atatgttaat atgtg 252034DNAartificialgfp-NheI-F forward primer 20ccaaaccgct agcaacatgg tgagcaaggg cgag 342149DNAartificialgfp-SphI reverse primer 21aggaaagggc atgcttaacg cgtaccggtc ttgtacagct cgtccatgc 492240DNAartificialpvp80-StuI-F forward primer 22ggaacaaagg cctgagctca aagtaagacc tttactgtcc 402335DNAartificialvp80-XbaI-R reverse primer 23ccttctatct agattatata acattgtagt ttgcg 352435DNAartificialvp80-SacI-F forward primer 24ttatcttgag ctcaatatga acgattccaa ttctc 352569DNAartificialvp80-FLAG-R1 reverse primer 25caacagagaa ttggaatcgt tcttatcgtc gtcatccttg taatccatat tataaggtta 60tatcgaatg 692662DNAartificialvp80-FLAG-R reverse primer 26ccttctatct agattactta tcgtcgtcat ccttgtaatc tataacattg tagtttgcgt 60tc 622723DNAartificialM13-F forward primer 27cccagtcacg acgttgtaaa acg 232823DNAartificialM13-R reverse primer 28agcggataac aatttcacac agg 232920DNAartificialGenR reverse primer 29agccacctac tcccaacatc 203071DNAartificialvp39-KO-F forward primer 30tcgggcacag acgcgaccag acccgtttcg tcaattatac acgtggcgca taccgttcgt 60ataatgtatg c 713170DNAartificialvp39-KO-R reverse primer 31gtttatttgc aacaaccacc tcataaaacg ttttaaaatg tcaaaaatgt accgttcgta 60tagcatacat 703233DNAartificialvp39-SacI-F forward primer 32aaggttctct agattagacg gctattcctc cac 333332DNAartificialvp39-XbaI-R reverse primer 33ttatcttgag ctcaatatgg cgctagtgcc cg 323439DNAartificialvp39-StuI-F forward primer 34ggaacaaagg cctgagctct tagacggcta ttcctccac 393534DNAartificiallef-4-XbaI-R reverse primer 35ccttctatct agattaattt ggcacgattc ggtc 343639DNAartificialcg-30-XbaI-F forward primer 36aaggttctct agattaatct acatttattg taacatttg 393761DNAartificialvp39-FLAG-SacI-R reverse primer 37ttatcttgag ctcaatatgg attacaagga tgacgacgat aaggcgctag tgcccgtggg 60t 613872DNAartificialvp1054-KO-F forward primer 38gtactgaaag ataatttatt tttgatagat aataattaca ttattttaaa cgtgttcgac 60caagaaaccg at 723945DNAartificialvp1054-KO-R1 reverse primer 39agggcgaatt ccagcacact ttattacgtg gacgcgttac tttgc 454071DNAartificialvp1054-KO-R2 reverse primer 40gataagaatg cttgtttaac aaataggtca gctgttaaat actggcgatg taccgttcgt 60atagcataca t 714141DNAartificialvp1054-Rep-F forward primer 41ggttgtttag gcctgagctc ctttggtacg tgttagagtg t 414236DNAartificialvp1054-Rep-R reverse primer 42tcctttcctc tagattacac gttgtgtgcg tgcaga 364367DNAartificialp6.9-KO-F forward primer 43gcttcgttca ttcgctactg tcggctgtgt ggaatgtctg gttgttaagt gtgctggaat 60tcgccct 674470DNAartificialp6.9-KO-R reverse primer 44aatattaata aggtaaaaat tacagctaca taaattacac aatttaaact accgttcgta 60tagcatacat 704532DNAartificialAc-p6.9-F forward primer 45tttgaattca tggttgcccg aagctccaag ac 324634DNAartificialAc-p6.9-R reverse primer 46tttgcggccg cttaatagta gcgtgttctg taac 344729DNAartificialSe-p6.9-F forward primer 47tttgaattca tgtatcgtcg tcgttcatc 294834DNAartificialSe-p6.9-R reverse primer 48tttgcggccg cttaatagtg gcgacgtctg tatc 344922DNAartificial86596 forward primer 49gggcttagtt taaaatcttg ca 225021DNAartificial86995 reverse primer 50aattcaaacg accaagacga g 215121DNAartificial45122 forward primer 51gcaatcatga cgaacgtatg g 215222DNAartificial46441 reverse primer 52cgataatttt tccaagcgct ac 225330DNAartificialpp6.9-F forward primer 53ggtcgacgta ccaaattccg ttttgcgacg 305434DNAartificialpp6.9-R reverse primer 54ggtcgacgga tccgtttaaa ttgtgtaatt tatg 345521DNAartificial75834 forward primer 55cttcttatcg ggttgtacaa c 215620DNAartificial76420 reverse primer 56gcgtatcatg acgatggatg 20

Claims

1. (canceled)

2. A method for the production of a biopharmaceutical product, comprising: (a) infecting a biopharmaceutical-producing insect cell with at least one baculovirus, said at least one baculovirus comprising a genome coding for said biopharmaceutical product, and (b) maintaining the biopharmaceutical-producing insect cell under conditions such that the biopharmaceutical product is produced, wherein the genome of said at least one baculovirus is deficient for the p6.9 gene or wherein said biopharmaceutical-producing insect cell comprises an expression control system allowing the inactivation of the p6.9 gene.

3. The method according to claim 2, wherein the p6.9 gene is made deficient in said genome by way of nucleotide substitution, insertion or deletion.

4. The method according to claim 2, wherein the biopharmaceutical-producing insect cell is a recombinant insect cell comprising a construct expressing a dsRNA specific for the p6.9 gene, the dsRNA being optionally expressed under an inducible promoter.

5. The method according to claim 2, wherein the at least one baculovirus is produced before step (a) in a baculovirus-producing cell expressing a complementing copy of the p6.9 gene.

6. The method according to claim 2, wherein the genome of said at least one baculovirus is further deficient for at least one gene selected from vp80, vp1054 and vp39 or wherein said biopharmaceutical-producing insect cell further comprises an expression control system allowing the inactivation of at least one gene selected from vp80, vp1054 and vp39.

7. The method according to claim 2, wherein the deficiency or inactivation of the p6.9 gene does not affect very late expression from said baculovirus in comparison to very late expression from wild-type baculovirus.

8. The method according to claim 2, wherein the at least one baculovirus is derived from AcMNPV or BmNPV.

9. The method according to claim 2, wherein the biopharmaceutical product is a recombinant protein, a recombinant virus or a virus-like particle.

10. The method according to claim 9, wherein the biopharmaceutical product is a recombinant AAV.

11. The method according to claim 2, wherein the biopharmaceutical product is coded by at least one gene introduced in the recombinant baculovirus genome under the control of the polyhedrin or p10 promoter.

12. A bacmid comprising a baculoviral genome, wherein said genome is deficient for the p6.9 gene.

13. The bacmid according to claim 12, wherein said genome is further deficient for at least one gene selected from vp80, vp1054 and vp39.

14. The bacmid according to claim 12, wherein said genome is derived from AcMNPV.

15. A recombinant baculovirus vector, wherein the genome of said baculovirus vector is deficient for the p6.9 gene.

16. The recombinant baculovirus vector according to claim 15, wherein the genome of said baculovirus is further deficient for at least one gene selected from vp80, vp1054 and vp39.

17. The recombinant baculovirus vector according to claim 15, wherein said vector is an AcMNPV baculovirus vector.

18. An insect cell infected with a recombinant baculovirus vector comprising a genome which is deficient for the p6.9 gene.

19. The insect cell according to claim 18, wherein said genome is further deficient for at least one gene selected from vp80, vp1054 and vp39.

20. The insect cell according to claim 18, wherein said genome is derived from AcMNPV.

21. An insect cell, comprising a construct expressing a dsRNA specific of the p6.9 gene.

22. The insect cell according to claim 21, wherein said construct is integrated in the genome of the insect cell.

23. The insect cell according to claim 21, wherein said insect cell further comprises a construct expressing a dsRNA specific of at least one gene selected from vp80, vp1054 and vp39.

24. A cell comprising an expression cassette coding for the p6.9 gene.

25. The cell according to claim 24, wherein said cell further comprises an expression cassette coding for at least one gene selected from vp80, vp1054 and vp39.

26. The cell according to claim 24, which is an insect cell.

27. A method for the production of a baculovirus deficient for the p6.9 gene, comprising the step of transfecting an insect cell comprising an expression cassette coding for the p6.9 gene with a bacmid comprising a baculoviral genome, wherein said genome is deficient for the p6.9 gene.

28. The method according to claim 27, wherein said insect cell further comprises an expression cassette coding for at least one gene selected from vp80, vp1054 and vp39 and wherein said baculoviral genome is further deficient for said at least one gene selected from vp80, vp1054 and vp39.